Canonical Allele Identifier: CA596781858

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 861048
• ClinVar RCV Id: RCV001067470
• dbSNP Id: rs1164486792
• gnomAD v2: 11-534294-CCCA-C
• gnomAD v4: 11-534294-CCCA-C
• MyVariant Identifiers: chr11:g.534295_534297del (hg19) ; chr11:g.534295_534297del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534304_534306del , CM000673.2:g.534304_534306del	GRCh38
NC_000011.9:g.534304_534306del , CM000673.1:g.534304_534306del	GRCh37
NC_000011.8:g.524304_524306del	NCBI36
NG_007666.1:g.6254_6256del

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.26_28del (HRAS)	ENSP00000380722.3:p.Val9del
ENST00000417302.7:c.26_28del (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Val9del
ENST00000417302.6:c.26_28del (HRAS)	ENSP00000388246.1:p.Val9del
ENST00000462734.2:c.26_28del (HRAS)	ENSP00000507303.1:p.Val9del
ENST00000311189.8:c.26_28del (HRAS) MANE Select	ENSP00000309845.7:p.Val9del
ENST00000311189.7:c.26_28del (HRAS)	ENSP00000309845.7:p.Val9del
ENST00000397594.5:c.26_28del (HRAS)	ENSP00000380722.1:p.Val9del
ENST00000397596.6:c.26_28del (HRAS)	ENSP00000380723.2:p.Val9del
ENST00000417302.5:c.26_28del (HRAS)	ENSP00000388246.1:p.Val9del
ENST00000451590.5:c.26_28del (HRAS)	ENSP00000407586.1:p.Val9del
ENST00000468682.2:n.514_516del (HRAS)
ENST00000482021.1:n.149_151del (HRAS)
ENST00000493230.5:c.26_28del (HRAS)	ENSP00000434023.1:p.Val9del
NM_001130442.1:c.26_28del (HRAS)	NP_001123914.1:p.Val9del
NM_005343.2:c.26_28del (HRAS)	NP_005334.1:p.Val9del
NM_176795.3:c.26_28del (HRAS)	NP_789765.1:p.Val9del
XM_011519875.1:c.-424-4294_-424-4292del (LRRC56)	XP_011518177.1:n.-424-4294_-424-4292del
XM_011519877.1:c.-161-5276_-161-5274del (LRRC56)	XP_011518179.1:n.-161-5276_-161-5274del
XR_242795.1:n.225_227del (HRAS)
NM_001130442.2:c.26_28del (HRAS)	NP_001123914.1:p.Val9del
NM_001318054.1:c.-294_-292del (HRAS)	NP_001304983.1:n.-294_-292del
NM_005343.3:c.26_28del (HRAS)	NP_005334.1:p.Val9del
NM_176795.4:c.26_28del (HRAS)	NP_789765.1:p.Val9del
XM_011519875.2:c.-424-4294_-424-4292del (LRRC56)	XP_011518177.1:n.-424-4294_-424-4292del
XM_011519877.2:c.-161-5276_-161-5274del (LRRC56)	XP_011518179.1:n.-161-5276_-161-5274del
XM_017017167.1:c.-499-4219_-499-4217del (LRRC56)	XP_016872656.1:n.-499-4219_-499-4217del
XM_017017168.1:c.-499-4219_-499-4217del (LRRC56)	XP_016872657.1:n.-499-4219_-499-4217del
NM_005343.4:c.26_28del (HRAS) MANE Select	NP_005334.1:p.Val9del
NM_001318054.2:c.-294_-292del (HRAS)	NP_001304983.1:n.-294_-292del
NM_001130442.3:c.26_28del (HRAS)	NP_001123914.1:p.Val9del
NM_176795.5:c.26_28del (HRAS) MANE Plus Clinical	NP_789765.1:p.Val9del