Canonical Allele Identifier: CA472322512

Gene: HRAS LRRC56

Linked Data

• MyVariant Identifiers: chr11:g.532741G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.532741G>T , CM000673.2:g.532741G>T	GRCh38
NC_000011.9:g.532741G>T , CM000673.1:g.532741G>T	GRCh37
NC_000011.8:g.522741G>T	NCBI36
NG_007666.1:g.7810C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.*20-111C>A (HRAS)	ENSP00000380722.3:n.*20-111C>A
ENST00000417302.7:c.*34C>A (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.*34C>A
ENST00000397594.6:c.251-111C>A (HRAS)	ENSP00000380722.2:n.251-111C>A
ENST00000417302.6:c.*34C>A (HRAS)	ENSP00000388246.1:n.*34C>A
ENST00000462734.2:c.*77C>A (HRAS)	ENSP00000507303.1:n.*77C>A
ENST00000311189.8:c.465C>A (HRAS) MANE Select	ENSP00000309845.7:p.Ala155=
ENST00000311189.7:c.465C>A (HRAS)	ENSP00000309845.7:p.Ala155=
ENST00000397594.5:c.*34C>A (HRAS)	ENSP00000380722.1:n.*34C>A
ENST00000397596.6:c.465C>A (HRAS)	ENSP00000380723.2:p.Ala155=
ENST00000417302.5:c.*34C>A (HRAS)	ENSP00000388246.1:n.*34C>A
ENST00000451590.5:c.465C>A (HRAS)	ENSP00000407586.1:p.Ala155=
ENST00000462734.1:n.240C>A (HRAS)
ENST00000478324.5:n.243-111C>A (HRAS)
ENST00000479482.1:n.386C>A (HRAS)
ENST00000493230.5:c.*34C>A (HRAS)	ENSP00000434023.1:n.*34C>A
NM_001130442.1:c.465C>A (HRAS)	NP_001123914.1:p.Ala155=
NM_005343.2:c.465C>A (HRAS)	NP_005334.1:p.Ala155=
NM_176795.3:c.*34C>A (HRAS)	NP_789765.1:n.*34C>A
XM_011519875.1:c.-425+4404G>T (LRRC56)	XP_011518177.1:n.-425+4404G>T
XM_011519877.1:c.-162+4404G>T (LRRC56)	XP_011518179.1:n.-162+4404G>T
XR_242795.1:n.746C>A (HRAS)
NM_001130442.2:c.465C>A (HRAS)	NP_001123914.1:p.Ala155=
NM_001318054.1:c.228C>A (HRAS)	NP_001304983.1:p.Ala76=
NM_005343.3:c.465C>A (HRAS)	NP_005334.1:p.Ala155=
NM_176795.4:c.*34C>A (HRAS)	NP_789765.1:n.*34C>A
XM_011519875.2:c.-425+4404G>T (LRRC56)	XP_011518177.1:n.-425+4404G>T
XM_011519877.2:c.-162+4404G>T (LRRC56)	XP_011518179.1:n.-162+4404G>T
XM_017017167.1:c.-500+4404G>T (LRRC56)	XP_016872656.1:n.-500+4404G>T
XM_017017168.1:c.-500+4404G>T (LRRC56)	XP_016872657.1:n.-500+4404G>T
NM_005343.4:c.465C>A (HRAS) MANE Select	NP_005334.1:p.Ala155=
NM_001318054.2:c.228C>A (HRAS)	NP_001304983.1:p.Ala76=
NM_001130442.3:c.465C>A (HRAS)	NP_001123914.1:p.Ala155=
NM_176795.5:c.*34C>A (HRAS) MANE Plus Clinical	NP_789765.1:n.*34C>A