Canonical Allele Identifier: CA296077

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 40430
• ClinVar RCV Id: RCV000157929
• dbSNP Id: rs727503094
• MyVariant Identifiers: chr11:g.534287_534288delinsAG (hg19) ; chr11:g.534287_534288delinsAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534287_534288delinsAG , CM000673.2:g.534287_534288delinsAG	GRCh38
NC_000011.9:g.534287_534288delinsAG , CM000673.1:g.534287_534288delinsAG	GRCh37
NC_000011.8:g.524287_524288delinsAG	NCBI36
NG_007666.1:g.6263_6264delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.35_36delinsCT (HRAS)	ENSP00000380722.3:p.Gly12Ala
ENST00000417302.7:c.35_36delinsCT (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Gly12Ala
ENST00000417302.6:c.35_36delinsCT (HRAS)	ENSP00000388246.1:p.Gly12Ala
ENST00000462734.2:c.35_36delinsCT (HRAS)	ENSP00000507303.1:p.Gly12Ala
ENST00000311189.8:c.35_36delinsCT (HRAS) MANE Select	ENSP00000309845.7:p.Gly12Ala
ENST00000311189.7:c.35_36delinsCT (HRAS)	ENSP00000309845.7:p.Gly12Ala
ENST00000397594.5:c.35_36delinsCT (HRAS)	ENSP00000380722.1:p.Gly12Ala
ENST00000397596.6:c.35_36delinsCT (HRAS)	ENSP00000380723.2:p.Gly12Ala
ENST00000417302.5:c.35_36delinsCT (HRAS)	ENSP00000388246.1:p.Gly12Ala
ENST00000451590.5:c.35_36delinsCT (HRAS)	ENSP00000407586.1:p.Gly12Ala
ENST00000468682.2:n.523_524delinsCT (HRAS)
ENST00000482021.1:n.158_159delinsCT (HRAS)
ENST00000493230.5:c.35_36delinsCT (HRAS)	ENSP00000434023.1:p.Gly12Ala
NM_001130442.1:c.35_36delinsCT (HRAS)	NP_001123914.1:p.Gly12Ala
NM_005343.2:c.35_36delinsCT (HRAS)	NP_005334.1:p.Gly12Ala
NM_176795.3:c.35_36delinsCT (HRAS)	NP_789765.1:p.Gly12Ala
XM_011519875.1:c.-424-4311_-424-4310delinsAG (LRRC56)	XP_011518177.1:n.-424-4311_-424-4310delinsAG
XM_011519877.1:c.-161-5293_-161-5292delinsAG (LRRC56)	XP_011518179.1:n.-161-5293_-161-5292delinsAG
XR_242795.1:n.234_235delinsCT (HRAS)
NM_001130442.2:c.35_36delinsCT (HRAS)	NP_001123914.1:p.Gly12Ala
NM_001318054.1:c.-285_-284delinsCT (HRAS)	NP_001304983.1:n.-285_-284delinsCT
NM_005343.3:c.35_36delinsCT (HRAS)	NP_005334.1:p.Gly12Ala
NM_176795.4:c.35_36delinsCT (HRAS)	NP_789765.1:p.Gly12Ala
XM_011519875.2:c.-424-4311_-424-4310delinsAG (LRRC56)	XP_011518177.1:n.-424-4311_-424-4310delinsAG
XM_011519877.2:c.-161-5293_-161-5292delinsAG (LRRC56)	XP_011518179.1:n.-161-5293_-161-5292delinsAG
XM_017017167.1:c.-499-4236_-499-4235delinsAG (LRRC56)	XP_016872656.1:n.-499-4236_-499-4235delinsAG
XM_017017168.1:c.-499-4236_-499-4235delinsAG (LRRC56)	XP_016872657.1:n.-499-4236_-499-4235delinsAG
NM_005343.4:c.35_36delinsCT (HRAS) MANE Select	NP_005334.1:p.Gly12Ala
NM_001318054.2:c.-285_-284delinsCT (HRAS)	NP_001304983.1:n.-285_-284delinsCT
NM_001130442.3:c.35_36delinsCT (HRAS)	NP_001123914.1:p.Gly12Ala
NM_176795.5:c.35_36delinsCT (HRAS) MANE Plus Clinical	NP_789765.1:p.Gly12Ala