Canonical Allele Identifier: CA5779264

Gene: HRAS LRRC56

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533328C>T , CM000673.2:g.533328C>T	GRCh38
NC_000011.9:g.533328C>T , CM000673.1:g.533328C>T	GRCh37
NC_000011.8:g.523328C>T	NCBI36
NG_007666.1:g.7223G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005343.4:c.450+125G>A (HRAS) MANE Select	NP_005334.1:n.450+125G>A
ENST00000311189.8:c.450+125G>A (HRAS) MANE Select	ENSP00000309845.7:n.450+125G>A
NM_176795.5:c.481G>A (HRAS) MANE Plus Clinical	NP_789765.1:p.Gly161Arg
ENST00000417302.7:c.481G>A (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Gly161Arg
NM_001130442.1:c.450+125G>A (HRAS)	NP_001123914.1:n.450+125G>A
NM_001130442.2:c.450+125G>A (HRAS)	NP_001123914.1:n.450+125G>A
NM_001130442.3:c.450+125G>A (HRAS)	NP_001123914.1:n.450+125G>A
NM_001318054.1:c.162G>A (HRAS)	NP_001304983.1:p.Pro54=
NM_001318054.2:c.162G>A (HRAS)	NP_001304983.1:p.Pro54=
NM_005343.2:c.450+125G>A (HRAS)	NP_005334.1:n.450+125G>A
NM_005343.3:c.450+125G>A (HRAS)	NP_005334.1:n.450+125G>A
NM_176795.3:c.481G>A (HRAS)	NP_789765.1:p.Gly161Arg
NM_176795.4:c.481G>A (HRAS)	NP_789765.1:p.Gly161Arg
ENST00000311189.7:c.450+125G>A (HRAS)	ENSP00000309845.7:n.450+125G>A
ENST00000397594.5:c.481G>A (HRAS)	ENSP00000380722.1:p.Gly161Arg
ENST00000397594.6:c.199G>A (HRAS)	ENSP00000380722.2:p.Gly67Arg
ENST00000397594.7:c.481G>A (HRAS)	ENSP00000380722.3:p.Gly161Arg
ENST00000397596.6:c.450+125G>A (HRAS)	ENSP00000380723.2:n.450+125G>A
ENST00000417302.5:c.481G>A (HRAS)	ENSP00000388246.1:p.Gly161Arg
ENST00000417302.6:c.481G>A (HRAS)	ENSP00000388246.1:p.Gly161Arg
ENST00000451590.5:c.450+125G>A (HRAS)	ENSP00000407586.1:n.450+125G>A
ENST00000462734.1:n.174G>A (HRAS)
ENST00000462734.2:c.*11G>A (HRAS)	ENSP00000507303.1:n.*11G>A
ENST00000478324.5:n.191G>A (HRAS)
ENST00000479482.1:n.371+125G>A (HRAS)
ENST00000493230.5:c.481G>A (HRAS)	ENSP00000434023.1:p.Gly161Arg
XM_011519875.1:c.-425+4991C>T (LRRC56)	XP_011518177.1:n.-425+4991C>T
XM_011519875.2:c.-425+4991C>T (LRRC56)	XP_011518177.1:n.-425+4991C>T
XM_011519877.1:c.-162+4991C>T (LRRC56)	XP_011518179.1:n.-162+4991C>T
XM_011519877.2:c.-162+4991C>T (LRRC56)	XP_011518179.1:n.-162+4991C>T
XM_017017167.1:c.-500+4991C>T (LRRC56)	XP_016872656.1:n.-500+4991C>T
XM_017017168.1:c.-500+4991C>T (LRRC56)	XP_016872657.1:n.-500+4991C>T
XR_242795.1:n.680G>A (HRAS)