Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.532467_532471delinsCTCCT , CM000673.2:g.532467_532471delinsCTCCT	GRCh38
NC_000011.9:g.532467_532471delinsCTCCT , CM000673.1:g.532467_532471delinsCTCCT	GRCh37
NC_000011.8:g.522467_522471delinsCTCCT	NCBI36
NG_007666.1:g.8080_8084delinsAGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.179_183delinsAGGAG (HRAS)	ENSP00000380722.3:n.179_183delinsAGGAG
ENST00000417302.7:c.304_308delinsAGGAG (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.304_308delinsAGGAG
ENST00000397594.6:c.410_414delinsAGGAG (HRAS)	ENSP00000380722.2:n.410_414delinsAGGAG
ENST00000417302.6:c.304_308delinsAGGAG (HRAS)	ENSP00000388246.1:n.304_308delinsAGGAG
ENST00000462734.2:c.239_243delinsAGGAG (HRAS)	ENSP00000507303.1:n.239_243delinsAGGAG
ENST00000311189.8:c.57_61delinsAGGAG (HRAS) MANE Select	ENSP00000309845.7:n.57_61delinsAGGAG
ENST00000311189.7:c.57_61delinsAGGAG (HRAS)	ENSP00000309845.7:n.57_61delinsAGGAG
ENST00000397594.5:c.304_308delinsAGGAG (HRAS)	ENSP00000380722.1:n.304_308delinsAGGAG
ENST00000397596.6:c.165_169delinsAGGAG (HRAS)	ENSP00000380723.2:n.165_169delinsAGGAG
ENST00000417302.5:c.304_308delinsAGGAG (HRAS)	ENSP00000388246.1:n.304_308delinsAGGAG
ENST00000451590.5:c.165_169delinsAGGAG (HRAS)	ENSP00000407586.1:n.165_169delinsAGGAG
ENST00000462734.1:n.402_406delinsAGGAG (HRAS)
ENST00000478324.5:n.402_406delinsAGGAG (HRAS)
ENST00000493230.5:c.196_200delinsAGGAG (HRAS)	ENSP00000434023.1:n.196_200delinsAGGAG
NM_001130442.1:c.165_169delinsAGGAG (HRAS)	NP_001123914.1:n.165_169delinsAGGAG
NM_005343.2:c.57_61delinsAGGAG (HRAS)	NP_005334.1:n.57_61delinsAGGAG
NM_176795.3:c.304_308delinsAGGAG (HRAS)	NP_789765.1:n.304_308delinsAGGAG
XM_011519875.1:c.-425+4130_-425+4134delinsCTCCT (LRRC56)	XP_011518177.1:n.-425+4130_-425+4134delinsCTCCT
XM_011519877.1:c.-162+4130_-162+4134delinsCTCCT (LRRC56)	XP_011518179.1:n.-162+4130_-162+4134delinsCTCCT
XR_242795.1:n.908_912delinsAGGAG (HRAS)
NM_001130442.2:c.165_169delinsAGGAG (HRAS)	NP_001123914.1:n.165_169delinsAGGAG
NM_001318054.1:c.57_61delinsAGGAG (HRAS)	NP_001304983.1:n.57_61delinsAGGAG
NM_005343.3:c.57_61delinsAGGAG (HRAS)	NP_005334.1:n.57_61delinsAGGAG
NM_176795.4:c.304_308delinsAGGAG (HRAS)	NP_789765.1:n.304_308delinsAGGAG
XM_011519875.2:c.-425+4130_-425+4134delinsCTCCT (LRRC56)	XP_011518177.1:n.-425+4130_-425+4134delinsCTCCT
XM_011519877.2:c.-162+4130_-162+4134delinsCTCCT (LRRC56)	XP_011518179.1:n.-162+4130_-162+4134delinsCTCCT
XM_017017167.1:c.-500+4130_-500+4134delinsCTCCT (LRRC56)	XP_016872656.1:n.-500+4130_-500+4134delinsCTCCT
XM_017017168.1:c.-500+4130_-500+4134delinsCTCCT (LRRC56)	XP_016872657.1:n.-500+4130_-500+4134delinsCTCCT
NM_005343.4:c.57_61delinsAGGAG (HRAS) MANE Select	NP_005334.1:n.57_61delinsAGGAG
NM_001318054.2:c.57_61delinsAGGAG (HRAS)	NP_001304983.1:n.57_61delinsAGGAG
NM_001130442.3:c.165_169delinsAGGAG (HRAS)	NP_001123914.1:n.165_169delinsAGGAG
NM_176795.5:c.304_308delinsAGGAG (HRAS) MANE Plus Clinical	NP_789765.1:n.304_308delinsAGGAG

HGVS	Amino-acid Change
ENST00000397594.7:c.179_183delinsAGGAG (HRAS)	ENSP00000380722.3:n.179_183delinsAGGAG
ENST00000417302.7:c.304_308delinsAGGAG (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.304_308delinsAGGAG
ENST00000397594.6:c.410_414delinsAGGAG (HRAS)	ENSP00000380722.2:n.410_414delinsAGGAG
ENST00000417302.6:c.304_308delinsAGGAG (HRAS)	ENSP00000388246.1:n.304_308delinsAGGAG
ENST00000462734.2:c.239_243delinsAGGAG (HRAS)	ENSP00000507303.1:n.239_243delinsAGGAG
ENST00000311189.8:c.57_61delinsAGGAG (HRAS) MANE Select	ENSP00000309845.7:n.57_61delinsAGGAG
ENST00000311189.7:c.57_61delinsAGGAG (HRAS)	ENSP00000309845.7:n.57_61delinsAGGAG
ENST00000397594.5:c.304_308delinsAGGAG (HRAS)	ENSP00000380722.1:n.304_308delinsAGGAG
ENST00000397596.6:c.165_169delinsAGGAG (HRAS)	ENSP00000380723.2:n.165_169delinsAGGAG
ENST00000417302.5:c.304_308delinsAGGAG (HRAS)	ENSP00000388246.1:n.304_308delinsAGGAG
ENST00000451590.5:c.165_169delinsAGGAG (HRAS)	ENSP00000407586.1:n.165_169delinsAGGAG
ENST00000462734.1:n.402_406delinsAGGAG (HRAS)
ENST00000478324.5:n.402_406delinsAGGAG (HRAS)
ENST00000493230.5:c.196_200delinsAGGAG (HRAS)	ENSP00000434023.1:n.196_200delinsAGGAG
NM_001130442.1:c.165_169delinsAGGAG (HRAS)	NP_001123914.1:n.165_169delinsAGGAG
NM_005343.2:c.57_61delinsAGGAG (HRAS)	NP_005334.1:n.57_61delinsAGGAG
NM_176795.3:c.304_308delinsAGGAG (HRAS)	NP_789765.1:n.304_308delinsAGGAG
XM_011519875.1:c.-425+4130_-425+4134delinsCTCCT (LRRC56)	XP_011518177.1:n.-425+4130_-425+4134delinsCTCCT
XM_011519877.1:c.-162+4130_-162+4134delinsCTCCT (LRRC56)	XP_011518179.1:n.-162+4130_-162+4134delinsCTCCT
XR_242795.1:n.908_912delinsAGGAG (HRAS)
NM_001130442.2:c.165_169delinsAGGAG (HRAS)	NP_001123914.1:n.165_169delinsAGGAG
NM_001318054.1:c.57_61delinsAGGAG (HRAS)	NP_001304983.1:n.57_61delinsAGGAG
NM_005343.3:c.57_61delinsAGGAG (HRAS)	NP_005334.1:n.57_61delinsAGGAG
NM_176795.4:c.304_308delinsAGGAG (HRAS)	NP_789765.1:n.304_308delinsAGGAG
XM_011519875.2:c.-425+4130_-425+4134delinsCTCCT (LRRC56)	XP_011518177.1:n.-425+4130_-425+4134delinsCTCCT
XM_011519877.2:c.-162+4130_-162+4134delinsCTCCT (LRRC56)	XP_011518179.1:n.-162+4130_-162+4134delinsCTCCT
XM_017017167.1:c.-500+4130_-500+4134delinsCTCCT (LRRC56)	XP_016872656.1:n.-500+4130_-500+4134delinsCTCCT
XM_017017168.1:c.-500+4130_-500+4134delinsCTCCT (LRRC56)	XP_016872657.1:n.-500+4130_-500+4134delinsCTCCT
NM_005343.4:c.57_61delinsAGGAG (HRAS) MANE Select	NP_005334.1:n.57_61delinsAGGAG
NM_001318054.2:c.57_61delinsAGGAG (HRAS)	NP_001304983.1:n.57_61delinsAGGAG
NM_001130442.3:c.165_169delinsAGGAG (HRAS)	NP_001123914.1:n.165_169delinsAGGAG
NM_176795.5:c.304_308delinsAGGAG (HRAS) MANE Plus Clinical	NP_789765.1:n.304_308delinsAGGAG