Canonical Allele Identifier: CA10603217

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 279921
• ClinVar RCV Id: RCV000322736
• dbSNP Id: rs727503094
• MyVariant Identifiers: chr11:g.534287_534288delinsTA (hg19) ; chr11:g.534287_534288delinsTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534287_534288delinsTA , CM000673.2:g.534287_534288delinsTA	GRCh38
NC_000011.9:g.534287_534288delinsTA , CM000673.1:g.534287_534288delinsTA	GRCh37
NC_000011.8:g.524287_524288delinsTA	NCBI36
NG_007666.1:g.6263_6264delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.35_36delinsTA (HRAS)	ENSP00000380722.3:p.Gly12Val
ENST00000417302.7:c.35_36delinsTA (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Gly12Val
ENST00000417302.6:c.35_36delinsTA (HRAS)	ENSP00000388246.1:p.Gly12Val
ENST00000462734.2:c.35_36delinsTA (HRAS)	ENSP00000507303.1:p.Gly12Val
ENST00000311189.8:c.35_36delinsTA (HRAS) MANE Select	ENSP00000309845.7:p.Gly12Val
ENST00000311189.7:c.35_36delinsTA (HRAS)	ENSP00000309845.7:p.Gly12Val
ENST00000397594.5:c.35_36delinsTA (HRAS)	ENSP00000380722.1:p.Gly12Val
ENST00000397596.6:c.35_36delinsTA (HRAS)	ENSP00000380723.2:p.Gly12Val
ENST00000417302.5:c.35_36delinsTA (HRAS)	ENSP00000388246.1:p.Gly12Val
ENST00000451590.5:c.35_36delinsTA (HRAS)	ENSP00000407586.1:p.Gly12Val
ENST00000468682.2:n.523_524delinsTA (HRAS)
ENST00000482021.1:n.158_159delinsTA (HRAS)
ENST00000493230.5:c.35_36delinsTA (HRAS)	ENSP00000434023.1:p.Gly12Val
NM_001130442.1:c.35_36delinsTA (HRAS)	NP_001123914.1:p.Gly12Val
NM_005343.2:c.35_36delinsTA (HRAS)	NP_005334.1:p.Gly12Val
NM_176795.3:c.35_36delinsTA (HRAS)	NP_789765.1:p.Gly12Val
XM_011519875.1:c.-424-4311_-424-4310delinsTA (LRRC56)	XP_011518177.1:n.-424-4311_-424-4310delinsTA
XM_011519877.1:c.-161-5293_-161-5292delinsTA (LRRC56)	XP_011518179.1:n.-161-5293_-161-5292delinsTA
XR_242795.1:n.234_235delinsTA (HRAS)
NM_001130442.2:c.35_36delinsTA (HRAS)	NP_001123914.1:p.Gly12Val
NM_001318054.1:c.-285_-284delinsTA (HRAS)	NP_001304983.1:n.-285_-284delinsTA
NM_005343.3:c.35_36delinsTA (HRAS)	NP_005334.1:p.Gly12Val
NM_176795.4:c.35_36delinsTA (HRAS)	NP_789765.1:p.Gly12Val
XM_011519875.2:c.-424-4311_-424-4310delinsTA (LRRC56)	XP_011518177.1:n.-424-4311_-424-4310delinsTA
XM_011519877.2:c.-161-5293_-161-5292delinsTA (LRRC56)	XP_011518179.1:n.-161-5293_-161-5292delinsTA
XM_017017167.1:c.-499-4236_-499-4235delinsTA (LRRC56)	XP_016872656.1:n.-499-4236_-499-4235delinsTA
XM_017017168.1:c.-499-4236_-499-4235delinsTA (LRRC56)	XP_016872657.1:n.-499-4236_-499-4235delinsTA
NM_005343.4:c.35_36delinsTA (HRAS) MANE Select	NP_005334.1:p.Gly12Val
NM_001318054.2:c.-285_-284delinsTA (HRAS)	NP_001304983.1:n.-285_-284delinsTA
NM_001130442.3:c.35_36delinsTA (HRAS)	NP_001123914.1:p.Gly12Val
NM_176795.5:c.35_36delinsTA (HRAS) MANE Plus Clinical	NP_789765.1:p.Gly12Val