Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.532430_532434delinsCCCTT , CM000673.2:g.532430_532434delinsCCCTT	GRCh38
NC_000011.9:g.532430_532434delinsCCCTT , CM000673.1:g.532430_532434delinsCCCTT	GRCh37
NC_000011.8:g.522430_522434delinsCCCTT	NCBI36
NG_007666.1:g.8117_8121delinsAAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.216_220delinsAAGGG (HRAS)	ENSP00000380722.3:n.216_220delinsAAGGG
ENST00000417302.7:c.341_345delinsAAGGG (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.341_345delinsAAGGG
ENST00000397594.6:c.447_451delinsAAGGG (HRAS)	ENSP00000380722.2:n.447_451delinsAAGGG
ENST00000417302.6:c.341_345delinsAAGGG (HRAS)	ENSP00000388246.1:n.341_345delinsAAGGG
ENST00000462734.2:c.276_280delinsAAGGG (HRAS)	ENSP00000507303.1:n.276_280delinsAAGGG
ENST00000311189.8:c.94_98delinsAAGGG (HRAS) MANE Select	ENSP00000309845.7:n.94_98delinsAAGGG
ENST00000311189.7:c.94_98delinsAAGGG (HRAS)	ENSP00000309845.7:n.94_98delinsAAGGG
ENST00000397594.5:c.341_345delinsAAGGG (HRAS)	ENSP00000380722.1:n.341_345delinsAAGGG
ENST00000397596.6:c.202_206delinsAAGGG (HRAS)	ENSP00000380723.2:n.202_206delinsAAGGG
ENST00000417302.5:c.341_345delinsAAGGG (HRAS)	ENSP00000388246.1:n.341_345delinsAAGGG
ENST00000451590.5:c.202_206delinsAAGGG (HRAS)	ENSP00000407586.1:n.202_206delinsAAGGG
ENST00000462734.1:n.439_443delinsAAGGG (HRAS)
ENST00000478324.5:n.439_443delinsAAGGG (HRAS)
ENST00000493230.5:c.233_237delinsAAGGG (HRAS)	ENSP00000434023.1:n.233_237delinsAAGGG
NM_001130442.1:c.202_206delinsAAGGG (HRAS)	NP_001123914.1:n.202_206delinsAAGGG
NM_005343.2:c.94_98delinsAAGGG (HRAS)	NP_005334.1:n.94_98delinsAAGGG
NM_176795.3:c.341_345delinsAAGGG (HRAS)	NP_789765.1:n.341_345delinsAAGGG
XM_011519875.1:c.-425+4093_-425+4097delinsCCCTT (LRRC56)	XP_011518177.1:n.-425+4093_-425+4097delinsCCCTT
XM_011519877.1:c.-162+4093_-162+4097delinsCCCTT (LRRC56)	XP_011518179.1:n.-162+4093_-162+4097delinsCCCTT
XR_242795.1:n.945_949delinsAAGGG (HRAS)
NM_001130442.2:c.202_206delinsAAGGG (HRAS)	NP_001123914.1:n.202_206delinsAAGGG
NM_001318054.1:c.94_98delinsAAGGG (HRAS)	NP_001304983.1:n.94_98delinsAAGGG
NM_005343.3:c.94_98delinsAAGGG (HRAS)	NP_005334.1:n.94_98delinsAAGGG
NM_176795.4:c.341_345delinsAAGGG (HRAS)	NP_789765.1:n.341_345delinsAAGGG
XM_011519875.2:c.-425+4093_-425+4097delinsCCCTT (LRRC56)	XP_011518177.1:n.-425+4093_-425+4097delinsCCCTT
XM_011519877.2:c.-162+4093_-162+4097delinsCCCTT (LRRC56)	XP_011518179.1:n.-162+4093_-162+4097delinsCCCTT
XM_017017167.1:c.-500+4093_-500+4097delinsCCCTT (LRRC56)	XP_016872656.1:n.-500+4093_-500+4097delinsCCCTT
XM_017017168.1:c.-500+4093_-500+4097delinsCCCTT (LRRC56)	XP_016872657.1:n.-500+4093_-500+4097delinsCCCTT
NM_005343.4:c.94_98delinsAAGGG (HRAS) MANE Select	NP_005334.1:n.94_98delinsAAGGG
NM_001318054.2:c.94_98delinsAAGGG (HRAS)	NP_001304983.1:n.94_98delinsAAGGG
NM_001130442.3:c.202_206delinsAAGGG (HRAS)	NP_001123914.1:n.202_206delinsAAGGG
NM_176795.5:c.341_345delinsAAGGG (HRAS) MANE Plus Clinical	NP_789765.1:n.341_345delinsAAGGG

HGVS	Amino-acid Change
ENST00000397594.7:c.216_220delinsAAGGG (HRAS)	ENSP00000380722.3:n.216_220delinsAAGGG
ENST00000417302.7:c.341_345delinsAAGGG (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.341_345delinsAAGGG
ENST00000397594.6:c.447_451delinsAAGGG (HRAS)	ENSP00000380722.2:n.447_451delinsAAGGG
ENST00000417302.6:c.341_345delinsAAGGG (HRAS)	ENSP00000388246.1:n.341_345delinsAAGGG
ENST00000462734.2:c.276_280delinsAAGGG (HRAS)	ENSP00000507303.1:n.276_280delinsAAGGG
ENST00000311189.8:c.94_98delinsAAGGG (HRAS) MANE Select	ENSP00000309845.7:n.94_98delinsAAGGG
ENST00000311189.7:c.94_98delinsAAGGG (HRAS)	ENSP00000309845.7:n.94_98delinsAAGGG
ENST00000397594.5:c.341_345delinsAAGGG (HRAS)	ENSP00000380722.1:n.341_345delinsAAGGG
ENST00000397596.6:c.202_206delinsAAGGG (HRAS)	ENSP00000380723.2:n.202_206delinsAAGGG
ENST00000417302.5:c.341_345delinsAAGGG (HRAS)	ENSP00000388246.1:n.341_345delinsAAGGG
ENST00000451590.5:c.202_206delinsAAGGG (HRAS)	ENSP00000407586.1:n.202_206delinsAAGGG
ENST00000462734.1:n.439_443delinsAAGGG (HRAS)
ENST00000478324.5:n.439_443delinsAAGGG (HRAS)
ENST00000493230.5:c.233_237delinsAAGGG (HRAS)	ENSP00000434023.1:n.233_237delinsAAGGG
NM_001130442.1:c.202_206delinsAAGGG (HRAS)	NP_001123914.1:n.202_206delinsAAGGG
NM_005343.2:c.94_98delinsAAGGG (HRAS)	NP_005334.1:n.94_98delinsAAGGG
NM_176795.3:c.341_345delinsAAGGG (HRAS)	NP_789765.1:n.341_345delinsAAGGG
XM_011519875.1:c.-425+4093_-425+4097delinsCCCTT (LRRC56)	XP_011518177.1:n.-425+4093_-425+4097delinsCCCTT
XM_011519877.1:c.-162+4093_-162+4097delinsCCCTT (LRRC56)	XP_011518179.1:n.-162+4093_-162+4097delinsCCCTT
XR_242795.1:n.945_949delinsAAGGG (HRAS)
NM_001130442.2:c.202_206delinsAAGGG (HRAS)	NP_001123914.1:n.202_206delinsAAGGG
NM_001318054.1:c.94_98delinsAAGGG (HRAS)	NP_001304983.1:n.94_98delinsAAGGG
NM_005343.3:c.94_98delinsAAGGG (HRAS)	NP_005334.1:n.94_98delinsAAGGG
NM_176795.4:c.341_345delinsAAGGG (HRAS)	NP_789765.1:n.341_345delinsAAGGG
XM_011519875.2:c.-425+4093_-425+4097delinsCCCTT (LRRC56)	XP_011518177.1:n.-425+4093_-425+4097delinsCCCTT
XM_011519877.2:c.-162+4093_-162+4097delinsCCCTT (LRRC56)	XP_011518179.1:n.-162+4093_-162+4097delinsCCCTT
XM_017017167.1:c.-500+4093_-500+4097delinsCCCTT (LRRC56)	XP_016872656.1:n.-500+4093_-500+4097delinsCCCTT
XM_017017168.1:c.-500+4093_-500+4097delinsCCCTT (LRRC56)	XP_016872657.1:n.-500+4093_-500+4097delinsCCCTT
NM_005343.4:c.94_98delinsAAGGG (HRAS) MANE Select	NP_005334.1:n.94_98delinsAAGGG
NM_001318054.2:c.94_98delinsAAGGG (HRAS)	NP_001304983.1:n.94_98delinsAAGGG
NM_001130442.3:c.202_206delinsAAGGG (HRAS)	NP_001123914.1:n.202_206delinsAAGGG
NM_176795.5:c.341_345delinsAAGGG (HRAS) MANE Plus Clinical	NP_789765.1:n.341_345delinsAAGGG