Canonical Allele Identifier: CA378921217

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 936794
• ClinVar RCV Id: RCV001205671
• dbSNP Id: rs1171537215
• MyVariant Identifiers: chr11:g.532743C>A (hg19) ; chr11:g.532743C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.532743C>A , CM000673.2:g.532743C>A	GRCh38
NC_000011.9:g.532743C>A , CM000673.1:g.532743C>A	GRCh37
NC_000011.8:g.522743C>A	NCBI36
NG_007666.1:g.7808G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.*20-113G>T (HRAS)	ENSP00000380722.3:n.*20-113G>T
ENST00000417302.7:c.*32G>T (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.*32G>T
ENST00000397594.6:c.251-113G>T (HRAS)	ENSP00000380722.2:n.251-113G>T
ENST00000417302.6:c.*32G>T (HRAS)	ENSP00000388246.1:n.*32G>T
ENST00000462734.2:c.*75G>T (HRAS)	ENSP00000507303.1:n.*75G>T
ENST00000311189.8:c.463G>T (HRAS) MANE Select	ENSP00000309845.7:p.Ala155Ser
ENST00000311189.7:c.463G>T (HRAS)	ENSP00000309845.7:p.Ala155Ser
ENST00000397594.5:c.*32G>T (HRAS)	ENSP00000380722.1:n.*32G>T
ENST00000397596.6:c.463G>T (HRAS)	ENSP00000380723.2:p.Ala155Ser
ENST00000417302.5:c.*32G>T (HRAS)	ENSP00000388246.1:n.*32G>T
ENST00000451590.5:c.463G>T (HRAS)	ENSP00000407586.1:p.Ala155Ser
ENST00000462734.1:n.238G>T (HRAS)
ENST00000478324.5:n.243-113G>T (HRAS)
ENST00000479482.1:n.384G>T (HRAS)
ENST00000493230.5:c.*32G>T (HRAS)	ENSP00000434023.1:n.*32G>T
NM_001130442.1:c.463G>T (HRAS)	NP_001123914.1:p.Ala155Ser
NM_005343.2:c.463G>T (HRAS)	NP_005334.1:p.Ala155Ser
NM_176795.3:c.*32G>T (HRAS)	NP_789765.1:n.*32G>T
XM_011519875.1:c.-425+4406C>A (LRRC56)	XP_011518177.1:n.-425+4406C>A
XM_011519877.1:c.-162+4406C>A (LRRC56)	XP_011518179.1:n.-162+4406C>A
XR_242795.1:n.744G>T (HRAS)
NM_001130442.2:c.463G>T (HRAS)	NP_001123914.1:p.Ala155Ser
NM_001318054.1:c.226G>T (HRAS)	NP_001304983.1:p.Ala76Ser
NM_005343.3:c.463G>T (HRAS)	NP_005334.1:p.Ala155Ser
NM_176795.4:c.*32G>T (HRAS)	NP_789765.1:n.*32G>T
XM_011519875.2:c.-425+4406C>A (LRRC56)	XP_011518177.1:n.-425+4406C>A
XM_011519877.2:c.-162+4406C>A (LRRC56)	XP_011518179.1:n.-162+4406C>A
XM_017017167.1:c.-500+4406C>A (LRRC56)	XP_016872656.1:n.-500+4406C>A
XM_017017168.1:c.-500+4406C>A (LRRC56)	XP_016872657.1:n.-500+4406C>A
NM_005343.4:c.463G>T (HRAS) MANE Select	NP_005334.1:p.Ala155Ser
NM_001318054.2:c.226G>T (HRAS)	NP_001304983.1:p.Ala76Ser
NM_001130442.3:c.463G>T (HRAS)	NP_001123914.1:p.Ala155Ser
NM_176795.5:c.*32G>T (HRAS) MANE Plus Clinical	NP_789765.1:n.*32G>T