Canonical Allele Identifier: CA472429347

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 2565161
• ClinVar RCV Id: RCV003301684
• dbSNP Id: rs2133986364
• gnomAD v4: 11-533471-G-A
• MyVariant Identifiers: chr11:g.533471G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533471G>A , CM000673.2:g.533471G>A	GRCh38
NC_000011.9:g.533471G>A , CM000673.1:g.533471G>A	GRCh37
NC_000011.8:g.523471G>A	NCBI36
NG_007666.1:g.7080C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.432C>T (HRAS)	ENSP00000380722.3:p.Thr144=
ENST00000417302.7:c.432C>T (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Thr144=
ENST00000397594.6:c.150C>T (HRAS)	ENSP00000380722.2:p.Thr50=
ENST00000417302.6:c.432C>T (HRAS)	ENSP00000388246.1:p.Thr144=
ENST00000462734.2:c.432C>T (HRAS)	ENSP00000507303.1:p.Thr144=
ENST00000311189.8:c.432C>T (HRAS) MANE Select	ENSP00000309845.7:p.Thr144=
ENST00000311189.7:c.432C>T (HRAS)	ENSP00000309845.7:p.Thr144=
ENST00000397594.5:c.432C>T (HRAS)	ENSP00000380722.1:p.Thr144=
ENST00000397596.6:c.432C>T (HRAS)	ENSP00000380723.2:p.Thr144=
ENST00000417302.5:c.432C>T (HRAS)	ENSP00000388246.1:p.Thr144=
ENST00000451590.5:c.432C>T (HRAS)	ENSP00000407586.1:p.Thr144=
ENST00000462734.1:n.125C>T (HRAS)
ENST00000478324.5:n.142C>T (HRAS)
ENST00000479482.1:n.353C>T (HRAS)
ENST00000493230.5:c.432C>T (HRAS)	ENSP00000434023.1:p.Thr144=
NM_001130442.1:c.432C>T (HRAS)	NP_001123914.1:p.Thr144=
NM_005343.2:c.432C>T (HRAS)	NP_005334.1:p.Thr144=
NM_176795.3:c.432C>T (HRAS)	NP_789765.1:p.Thr144=
XM_011519875.1:c.-424-5127G>A (LRRC56)	XP_011518177.1:n.-424-5127G>A
XM_011519877.1:c.-162+5134G>A (LRRC56)	XP_011518179.1:n.-162+5134G>A
XR_242795.1:n.631C>T (HRAS)
NM_001130442.2:c.432C>T (HRAS)	NP_001123914.1:p.Thr144=
NM_001318054.1:c.113C>T (HRAS)	NP_001304983.1:p.Pro38Leu
NM_005343.3:c.432C>T (HRAS)	NP_005334.1:p.Thr144=
NM_176795.4:c.432C>T (HRAS)	NP_789765.1:p.Thr144=
XM_011519875.2:c.-424-5127G>A (LRRC56)	XP_011518177.1:n.-424-5127G>A
XM_011519877.2:c.-162+5134G>A (LRRC56)	XP_011518179.1:n.-162+5134G>A
XM_017017167.1:c.-499-5052G>A (LRRC56)	XP_016872656.1:n.-499-5052G>A
XM_017017168.1:c.-499-5052G>A (LRRC56)	XP_016872657.1:n.-499-5052G>A
NM_005343.4:c.432C>T (HRAS) MANE Select	NP_005334.1:p.Thr144=
NM_001318054.2:c.113C>T (HRAS)	NP_001304983.1:p.Pro38Leu
NM_001130442.3:c.432C>T (HRAS)	NP_001123914.1:p.Thr144=
NM_176795.5:c.432C>T (HRAS) MANE Plus Clinical	NP_789765.1:p.Thr144=