Canonical Allele Identifier: CA296072

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 180854
• ClinVar RCV Id: RCV001678586
• dbSNP Id: rs727503094
• MyVariant Identifiers: chr11:g.534287_534288delinsAT (hg19) ; chr11:g.534287_534288delinsAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534287_534288delinsAT , CM000673.2:g.534287_534288delinsAT	GRCh38
NC_000011.9:g.534287_534288delinsAT , CM000673.1:g.534287_534288delinsAT	GRCh37
NC_000011.8:g.524287_524288delinsAT	NCBI36
NG_007666.1:g.6263_6264delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.35_36delinsAT (HRAS)	ENSP00000380722.3:p.Gly12Asp
ENST00000417302.7:c.35_36delinsAT (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Gly12Asp
ENST00000417302.6:c.35_36delinsAT (HRAS)	ENSP00000388246.1:p.Gly12Asp
ENST00000462734.2:c.35_36delinsAT (HRAS)	ENSP00000507303.1:p.Gly12Asp
ENST00000311189.8:c.35_36delinsAT (HRAS) MANE Select	ENSP00000309845.7:p.Gly12Asp
ENST00000311189.7:c.35_36delinsAT (HRAS)	ENSP00000309845.7:p.Gly12Asp
ENST00000397594.5:c.35_36delinsAT (HRAS)	ENSP00000380722.1:p.Gly12Asp
ENST00000397596.6:c.35_36delinsAT (HRAS)	ENSP00000380723.2:p.Gly12Asp
ENST00000417302.5:c.35_36delinsAT (HRAS)	ENSP00000388246.1:p.Gly12Asp
ENST00000451590.5:c.35_36delinsAT (HRAS)	ENSP00000407586.1:p.Gly12Asp
ENST00000468682.2:n.523_524delinsAT (HRAS)
ENST00000482021.1:n.158_159delinsAT (HRAS)
ENST00000493230.5:c.35_36delinsAT (HRAS)	ENSP00000434023.1:p.Gly12Asp
NM_001130442.1:c.35_36delinsAT (HRAS)	NP_001123914.1:p.Gly12Asp
NM_005343.2:c.35_36delinsAT (HRAS)	NP_005334.1:p.Gly12Asp
NM_176795.3:c.35_36delinsAT (HRAS)	NP_789765.1:p.Gly12Asp
XM_011519875.1:c.-424-4311_-424-4310delinsAT (LRRC56)	XP_011518177.1:n.-424-4311_-424-4310delinsAT
XM_011519877.1:c.-161-5293_-161-5292delinsAT (LRRC56)	XP_011518179.1:n.-161-5293_-161-5292delinsAT
XR_242795.1:n.234_235delinsAT (HRAS)
NM_001130442.2:c.35_36delinsAT (HRAS)	NP_001123914.1:p.Gly12Asp
NM_001318054.1:c.-285_-284delinsAT (HRAS)	NP_001304983.1:n.-285_-284delinsAT
NM_005343.3:c.35_36delinsAT (HRAS)	NP_005334.1:p.Gly12Asp
NM_176795.4:c.35_36delinsAT (HRAS)	NP_789765.1:p.Gly12Asp
XM_011519875.2:c.-424-4311_-424-4310delinsAT (LRRC56)	XP_011518177.1:n.-424-4311_-424-4310delinsAT
XM_011519877.2:c.-161-5293_-161-5292delinsAT (LRRC56)	XP_011518179.1:n.-161-5293_-161-5292delinsAT
XM_017017167.1:c.-499-4236_-499-4235delinsAT (LRRC56)	XP_016872656.1:n.-499-4236_-499-4235delinsAT
XM_017017168.1:c.-499-4236_-499-4235delinsAT (LRRC56)	XP_016872657.1:n.-499-4236_-499-4235delinsAT
NM_005343.4:c.35_36delinsAT (HRAS) MANE Select	NP_005334.1:p.Gly12Asp
NM_001318054.2:c.-285_-284delinsAT (HRAS)	NP_001304983.1:n.-285_-284delinsAT
NM_001130442.3:c.35_36delinsAT (HRAS)	NP_001123914.1:p.Gly12Asp
NM_176795.5:c.35_36delinsAT (HRAS) MANE Plus Clinical	NP_789765.1:p.Gly12Asp