Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.532580_532589dup , CM000673.2:g.532580_532589dup	GRCh38
NC_000011.9:g.532580_532589dup , CM000673.1:g.532580_532589dup	GRCh37
NC_000011.8:g.522580_522589dup	NCBI36
NG_007666.1:g.7962_7971dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.61_70dup (HRAS)	ENSP00000380722.3:n.61_70dup
ENST00000417302.7:c.186_195dup (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.186_195dup
ENST00000397594.6:c.292_301dup (HRAS)	ENSP00000380722.2:n.292_301dup
ENST00000417302.6:c.186_195dup (HRAS)	ENSP00000388246.1:n.186_195dup
ENST00000462734.2:c.187+42_187+51dup (HRAS)	ENSP00000507303.1:n.187+42_187+51dup
ENST00000311189.8:c.5+42_5+51dup (HRAS) MANE Select	ENSP00000309845.7:n.5+42_5+51dup
ENST00000311189.7:c.5+42_5+51dup (HRAS)	ENSP00000309845.7:n.5+42_5+51dup
ENST00000397594.5:c.186_195dup (HRAS)	ENSP00000380722.1:n.186_195dup
ENST00000397596.6:c.47_56dup (HRAS)	ENSP00000380723.2:n.47_56dup
ENST00000417302.5:c.186_195dup (HRAS)	ENSP00000388246.1:n.186_195dup
ENST00000451590.5:c.47_56dup (HRAS)	ENSP00000407586.1:n.47_56dup
ENST00000462734.1:n.350+42_350+51dup (HRAS)
ENST00000478324.5:n.284_293dup (HRAS)
ENST00000493230.5:c.144+42_144+51dup (HRAS)	ENSP00000434023.1:n.144+42_144+51dup
NM_001130442.1:c.47_56dup (HRAS)	NP_001123914.1:n.47_56dup
NM_005343.2:c.5+42_5+51dup (HRAS)	NP_005334.1:n.5+42_5+51dup
NM_176795.3:c.186_195dup (HRAS)	NP_789765.1:n.186_195dup
XM_011519875.1:c.-425+4243_-425+4252dup (LRRC56)	XP_011518177.1:n.-425+4243_-425+4252dup
XM_011519877.1:c.-162+4243_-162+4252dup (LRRC56)	XP_011518179.1:n.-162+4243_-162+4252dup
XR_242795.1:n.856+42_856+51dup (HRAS)
NM_001130442.2:c.47_56dup (HRAS)	NP_001123914.1:n.47_56dup
NM_001318054.1:c.5+42_5+51dup (HRAS)	NP_001304983.1:n.5+42_5+51dup
NM_005343.3:c.5+42_5+51dup (HRAS)	NP_005334.1:n.5+42_5+51dup
NM_176795.4:c.186_195dup (HRAS)	NP_789765.1:n.186_195dup
XM_011519875.2:c.-425+4243_-425+4252dup (LRRC56)	XP_011518177.1:n.-425+4243_-425+4252dup
XM_011519877.2:c.-162+4243_-162+4252dup (LRRC56)	XP_011518179.1:n.-162+4243_-162+4252dup
XM_017017167.1:c.-500+4243_-500+4252dup (LRRC56)	XP_016872656.1:n.-500+4243_-500+4252dup
XM_017017168.1:c.-500+4243_-500+4252dup (LRRC56)	XP_016872657.1:n.-500+4243_-500+4252dup
NM_005343.4:c.5+42_5+51dup (HRAS) MANE Select	NP_005334.1:n.5+42_5+51dup
NM_001318054.2:c.5+42_5+51dup (HRAS)	NP_001304983.1:n.5+42_5+51dup
NM_001130442.3:c.47_56dup (HRAS)	NP_001123914.1:n.47_56dup
NM_176795.5:c.186_195dup (HRAS) MANE Plus Clinical	NP_789765.1:n.186_195dup

HGVS	Amino-acid Change
ENST00000397594.7:c.61_70dup (HRAS)	ENSP00000380722.3:n.61_70dup
ENST00000417302.7:c.186_195dup (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.186_195dup
ENST00000397594.6:c.292_301dup (HRAS)	ENSP00000380722.2:n.292_301dup
ENST00000417302.6:c.186_195dup (HRAS)	ENSP00000388246.1:n.186_195dup
ENST00000462734.2:c.187+42_187+51dup (HRAS)	ENSP00000507303.1:n.187+42_187+51dup
ENST00000311189.8:c.5+42_5+51dup (HRAS) MANE Select	ENSP00000309845.7:n.5+42_5+51dup
ENST00000311189.7:c.5+42_5+51dup (HRAS)	ENSP00000309845.7:n.5+42_5+51dup
ENST00000397594.5:c.186_195dup (HRAS)	ENSP00000380722.1:n.186_195dup
ENST00000397596.6:c.47_56dup (HRAS)	ENSP00000380723.2:n.47_56dup
ENST00000417302.5:c.186_195dup (HRAS)	ENSP00000388246.1:n.186_195dup
ENST00000451590.5:c.47_56dup (HRAS)	ENSP00000407586.1:n.47_56dup
ENST00000462734.1:n.350+42_350+51dup (HRAS)
ENST00000478324.5:n.284_293dup (HRAS)
ENST00000493230.5:c.144+42_144+51dup (HRAS)	ENSP00000434023.1:n.144+42_144+51dup
NM_001130442.1:c.47_56dup (HRAS)	NP_001123914.1:n.47_56dup
NM_005343.2:c.5+42_5+51dup (HRAS)	NP_005334.1:n.5+42_5+51dup
NM_176795.3:c.186_195dup (HRAS)	NP_789765.1:n.186_195dup
XM_011519875.1:c.-425+4243_-425+4252dup (LRRC56)	XP_011518177.1:n.-425+4243_-425+4252dup
XM_011519877.1:c.-162+4243_-162+4252dup (LRRC56)	XP_011518179.1:n.-162+4243_-162+4252dup
XR_242795.1:n.856+42_856+51dup (HRAS)
NM_001130442.2:c.47_56dup (HRAS)	NP_001123914.1:n.47_56dup
NM_001318054.1:c.5+42_5+51dup (HRAS)	NP_001304983.1:n.5+42_5+51dup
NM_005343.3:c.5+42_5+51dup (HRAS)	NP_005334.1:n.5+42_5+51dup
NM_176795.4:c.186_195dup (HRAS)	NP_789765.1:n.186_195dup
XM_011519875.2:c.-425+4243_-425+4252dup (LRRC56)	XP_011518177.1:n.-425+4243_-425+4252dup
XM_011519877.2:c.-162+4243_-162+4252dup (LRRC56)	XP_011518179.1:n.-162+4243_-162+4252dup
XM_017017167.1:c.-500+4243_-500+4252dup (LRRC56)	XP_016872656.1:n.-500+4243_-500+4252dup
XM_017017168.1:c.-500+4243_-500+4252dup (LRRC56)	XP_016872657.1:n.-500+4243_-500+4252dup
NM_005343.4:c.5+42_5+51dup (HRAS) MANE Select	NP_005334.1:n.5+42_5+51dup
NM_001318054.2:c.5+42_5+51dup (HRAS)	NP_001304983.1:n.5+42_5+51dup
NM_001130442.3:c.47_56dup (HRAS)	NP_001123914.1:n.47_56dup
NM_176795.5:c.186_195dup (HRAS) MANE Plus Clinical	NP_789765.1:n.186_195dup