Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.532596G>T , CM000673.2:g.532596G>T	GRCh38
NC_000011.9:g.532596G>T , CM000673.1:g.532596G>T	GRCh37
NC_000011.8:g.522596G>T	NCBI36
NG_007666.1:g.7955C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.*54C>A (HRAS)	ENSP00000380722.3:n.*54C>A
ENST00000417302.7:c.*179C>A (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.*179C>A
ENST00000397594.6:c.285C>A (HRAS)	ENSP00000380722.2:n.285C>A
ENST00000417302.6:c.*179C>A (HRAS)	ENSP00000388246.1:n.*179C>A
ENST00000462734.2:c.*187+35C>A (HRAS)	ENSP00000507303.1:n.*187+35C>A
ENST00000311189.8:c.*5+35C>A (HRAS) MANE Select	ENSP00000309845.7:n.*5+35C>A
ENST00000311189.7:c.*5+35C>A (HRAS)	ENSP00000309845.7:n.*5+35C>A
ENST00000397594.5:c.*179C>A (HRAS)	ENSP00000380722.1:n.*179C>A
ENST00000397596.6:c.*40C>A (HRAS)	ENSP00000380723.2:n.*40C>A
ENST00000417302.5:c.*179C>A (HRAS)	ENSP00000388246.1:n.*179C>A
ENST00000451590.5:c.*40C>A (HRAS)	ENSP00000407586.1:n.*40C>A
ENST00000462734.1:n.350+35C>A (HRAS)
ENST00000478324.5:n.277C>A (HRAS)
ENST00000493230.5:c.*144+35C>A (HRAS)	ENSP00000434023.1:n.*144+35C>A
NM_001130442.1:c.*40C>A (HRAS)	NP_001123914.1:n.*40C>A
NM_005343.2:c.*5+35C>A (HRAS)	NP_005334.1:n.*5+35C>A
NM_176795.3:c.*179C>A (HRAS)	NP_789765.1:n.*179C>A
XM_011519875.1:c.-425+4259G>T (LRRC56)	XP_011518177.1:n.-425+4259G>T
XM_011519877.1:c.-162+4259G>T (LRRC56)	XP_011518179.1:n.-162+4259G>T
XR_242795.1:n.856+35C>A (HRAS)
NM_001130442.2:c.*40C>A (HRAS)	NP_001123914.1:n.*40C>A
NM_001318054.1:c.*5+35C>A (HRAS)	NP_001304983.1:n.*5+35C>A
NM_005343.3:c.*5+35C>A (HRAS)	NP_005334.1:n.*5+35C>A
NM_176795.4:c.*179C>A (HRAS)	NP_789765.1:n.*179C>A
XM_011519875.2:c.-425+4259G>T (LRRC56)	XP_011518177.1:n.-425+4259G>T
XM_011519877.2:c.-162+4259G>T (LRRC56)	XP_011518179.1:n.-162+4259G>T
XM_017017167.1:c.-500+4259G>T (LRRC56)	XP_016872656.1:n.-500+4259G>T
XM_017017168.1:c.-500+4259G>T (LRRC56)	XP_016872657.1:n.-500+4259G>T
NM_005343.4:c.*5+35C>A (HRAS) MANE Select	NP_005334.1:n.*5+35C>A
NM_001318054.2:c.*5+35C>A (HRAS)	NP_001304983.1:n.*5+35C>A
NM_001130442.3:c.*40C>A (HRAS)	NP_001123914.1:n.*40C>A
NM_176795.5:c.*179C>A (HRAS) MANE Plus Clinical	NP_789765.1:n.*179C>A