Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.532469C= , CM000673.2:g.532469C=	GRCh38
NC_000011.9:g.532469C= , CM000673.1:g.532469C=	GRCh37
NC_000011.8:g.522469C=	NCBI36
NG_007666.1:g.8082G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.*181G= (HRAS)	ENSP00000380722.3:n.*181G=
ENST00000417302.7:c.*306G= (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.*306G=
ENST00000397594.6:c.412G= (HRAS)	ENSP00000380722.2:n.412G=
ENST00000417302.6:c.*306G= (HRAS)	ENSP00000388246.1:n.*306G=
ENST00000462734.2:c.*241G= (HRAS)	ENSP00000507303.1:n.*241G=
ENST00000311189.8:c.*59G= (HRAS) MANE Select	ENSP00000309845.7:n.*59G=
ENST00000311189.7:c.*59G= (HRAS)	ENSP00000309845.7:n.*59G=
ENST00000397594.5:c.*306G= (HRAS)	ENSP00000380722.1:n.*306G=
ENST00000397596.6:c.*167G= (HRAS)	ENSP00000380723.2:n.*167G=
ENST00000417302.5:c.*306G= (HRAS)	ENSP00000388246.1:n.*306G=
ENST00000451590.5:c.*167G= (HRAS)	ENSP00000407586.1:n.*167G=
ENST00000462734.1:n.404G= (HRAS)
ENST00000478324.5:n.404G= (HRAS)
ENST00000493230.5:c.*198G= (HRAS)	ENSP00000434023.1:n.*198G=
NM_001130442.1:c.*167G= (HRAS)	NP_001123914.1:n.*167G=
NM_005343.2:c.*59G= (HRAS)	NP_005334.1:n.*59G=
NM_176795.3:c.*306G= (HRAS)	NP_789765.1:n.*306G=
XM_011519875.1:c.-425+4132C= (LRRC56)	XP_011518177.1:n.-425+4132C=
XM_011519877.1:c.-162+4132C= (LRRC56)	XP_011518179.1:n.-162+4132C=
XR_242795.1:n.910G= (HRAS)
NM_001130442.2:c.*167G= (HRAS)	NP_001123914.1:n.*167G=
NM_001318054.1:c.*59G= (HRAS)	NP_001304983.1:n.*59G=
NM_005343.3:c.*59G= (HRAS)	NP_005334.1:n.*59G=
NM_176795.4:c.*306G= (HRAS)	NP_789765.1:n.*306G=
XM_011519875.2:c.-425+4132C= (LRRC56)	XP_011518177.1:n.-425+4132C=
XM_011519877.2:c.-162+4132C= (LRRC56)	XP_011518179.1:n.-162+4132C=
XM_017017167.1:c.-500+4132C= (LRRC56)	XP_016872656.1:n.-500+4132C=
XM_017017168.1:c.-500+4132C= (LRRC56)	XP_016872657.1:n.-500+4132C=
NM_005343.4:c.*59G= (HRAS) MANE Select	NP_005334.1:n.*59G=
NM_001318054.2:c.*59G= (HRAS)	NP_001304983.1:n.*59G=
NM_001130442.3:c.*167G= (HRAS)	NP_001123914.1:n.*167G=
NM_176795.5:c.*306G= (HRAS) MANE Plus Clinical	NP_789765.1:n.*306G=