Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.532536A= , CM000673.2:g.532536A=	GRCh38
NC_000011.9:g.532536A= , CM000673.1:g.532536A=	GRCh37
NC_000011.8:g.522536A=	NCBI36
NG_007666.1:g.8015T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.*114T= (HRAS)	ENSP00000380722.3:n.*114T=
ENST00000417302.7:c.*239T= (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.*239T=
ENST00000397594.6:c.345T= (HRAS)	ENSP00000380722.2:n.345T=
ENST00000417302.6:c.*239T= (HRAS)	ENSP00000388246.1:n.*239T=
ENST00000462734.2:c.*188-14T= (HRAS)	ENSP00000507303.1:n.*188-14T=
ENST00000311189.8:c.*6-14T= (HRAS) MANE Select	ENSP00000309845.7:n.*6-14T=
ENST00000311189.7:c.*6-14T= (HRAS)	ENSP00000309845.7:n.*6-14T=
ENST00000397594.5:c.*239T= (HRAS)	ENSP00000380722.1:n.*239T=
ENST00000397596.6:c.*100T= (HRAS)	ENSP00000380723.2:n.*100T=
ENST00000417302.5:c.*239T= (HRAS)	ENSP00000388246.1:n.*239T=
ENST00000451590.5:c.*100T= (HRAS)	ENSP00000407586.1:n.*100T=
ENST00000462734.1:n.351-14T= (HRAS)
ENST00000478324.5:n.337T= (HRAS)
ENST00000493230.5:c.*145-14T= (HRAS)	ENSP00000434023.1:n.*145-14T=
NM_001130442.1:c.*100T= (HRAS)	NP_001123914.1:n.*100T=
NM_005343.2:c.*6-14T= (HRAS)	NP_005334.1:n.*6-14T=
NM_176795.3:c.*239T= (HRAS)	NP_789765.1:n.*239T=
XM_011519875.1:c.-425+4199A= (LRRC56)	XP_011518177.1:n.-425+4199A=
XM_011519877.1:c.-162+4199A= (LRRC56)	XP_011518179.1:n.-162+4199A=
XR_242795.1:n.857-14T= (HRAS)
NM_001130442.2:c.*100T= (HRAS)	NP_001123914.1:n.*100T=
NM_001318054.1:c.*6-14T= (HRAS)	NP_001304983.1:n.*6-14T=
NM_005343.3:c.*6-14T= (HRAS)	NP_005334.1:n.*6-14T=
NM_176795.4:c.*239T= (HRAS)	NP_789765.1:n.*239T=
XM_011519875.2:c.-425+4199A= (LRRC56)	XP_011518177.1:n.-425+4199A=
XM_011519877.2:c.-162+4199A= (LRRC56)	XP_011518179.1:n.-162+4199A=
XM_017017167.1:c.-500+4199A= (LRRC56)	XP_016872656.1:n.-500+4199A=
XM_017017168.1:c.-500+4199A= (LRRC56)	XP_016872657.1:n.-500+4199A=
NM_005343.4:c.*6-14T= (HRAS) MANE Select	NP_005334.1:n.*6-14T=
NM_001318054.2:c.*6-14T= (HRAS)	NP_001304983.1:n.*6-14T=
NM_001130442.3:c.*100T= (HRAS)	NP_001123914.1:n.*100T=
NM_176795.5:c.*239T= (HRAS) MANE Plus Clinical	NP_789765.1:n.*239T=