Canonical Allele Identifier: CA5779443

Gene: HRAS LRRC56

Linked Data

• dbSNP Id: rs772989900
• ExAC: 11:534327 CCT / C
• gnomAD v2: 11-534327-CCT-C
• gnomAD v4: 11-534327-CCT-C
• MyVariant Identifiers: chr11:g.534328_534329del (hg19) ; chr11:g.534328_534329del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534329_534330del , CM000673.2:g.534329_534330del	GRCh38
NC_000011.9:g.534329_534330del , CM000673.1:g.534329_534330del	GRCh37
NC_000011.8:g.524329_524330del	NCBI36
NG_007666.1:g.6222_6223del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.-7_-6del (HRAS)	ENSP00000380722.3:n.-7_-6del
ENST00000417302.7:c.-7_-6del (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.-7_-6del
ENST00000417302.6:c.-7_-6del (HRAS)	ENSP00000388246.1:n.-7_-6del
ENST00000462734.2:c.-7_-6del (HRAS)	ENSP00000507303.1:n.-7_-6del
ENST00000311189.8:c.-7_-6del (HRAS) MANE Select	ENSP00000309845.7:n.-7_-6del
ENST00000311189.7:c.-7_-6del (HRAS)	ENSP00000309845.7:n.-7_-6del
ENST00000397594.5:c.-7_-6del (HRAS)	ENSP00000380722.1:n.-7_-6del
ENST00000397596.6:c.-7_-6del (HRAS)	ENSP00000380723.2:n.-7_-6del
ENST00000417302.5:c.-7_-6del (HRAS)	ENSP00000388246.1:n.-7_-6del
ENST00000451590.5:c.-7_-6del (HRAS)	ENSP00000407586.1:n.-7_-6del
ENST00000468682.2:n.482_483del (HRAS)
ENST00000482021.1:n.117_118del (HRAS)
ENST00000493230.5:c.-7_-6del (HRAS)	ENSP00000434023.1:n.-7_-6del
NM_001130442.1:c.-7_-6del (HRAS)	NP_001123914.1:n.-7_-6del
NM_005343.2:c.-7_-6del (HRAS)	NP_005334.1:n.-7_-6del
NM_176795.3:c.-7_-6del (HRAS)	NP_789765.1:n.-7_-6del
XM_011519875.1:c.-424-4269_-424-4268del (LRRC56)	XP_011518177.1:n.-424-4269_-424-4268del
XM_011519877.1:c.-161-5251_-161-5250del (LRRC56)	XP_011518179.1:n.-161-5251_-161-5250del
XR_242795.1:n.193_194del (HRAS)
NM_001130442.2:c.-7_-6del (HRAS)	NP_001123914.1:n.-7_-6del
NM_001318054.1:c.-326_-325del (HRAS)	NP_001304983.1:n.-326_-325del
NM_005343.3:c.-7_-6del (HRAS)	NP_005334.1:n.-7_-6del
NM_176795.4:c.-7_-6del (HRAS)	NP_789765.1:n.-7_-6del
XM_011519875.2:c.-424-4269_-424-4268del (LRRC56)	XP_011518177.1:n.-424-4269_-424-4268del
XM_011519877.2:c.-161-5251_-161-5250del (LRRC56)	XP_011518179.1:n.-161-5251_-161-5250del
XM_017017167.1:c.-499-4194_-499-4193del (LRRC56)	XP_016872656.1:n.-499-4194_-499-4193del
XM_017017168.1:c.-499-4194_-499-4193del (LRRC56)	XP_016872657.1:n.-499-4194_-499-4193del
NM_005343.4:c.-7_-6del (HRAS) MANE Select	NP_005334.1:n.-7_-6del
NM_001318054.2:c.-326_-325del (HRAS)	NP_001304983.1:n.-326_-325del
NM_001130442.3:c.-7_-6del (HRAS)	NP_001123914.1:n.-7_-6del
NM_176795.5:c.-7_-6del (HRAS) MANE Plus Clinical	NP_789765.1:n.-7_-6del