Canonical Allele Identifier: CA677774804

Gene: HRAS LRRC56

Linked Data

• dbSNP Id: rs1246233335
• gnomAD v3: 11-533685-ACAGGAGGCCCCTGCCTGGACG-A
• gnomAD v4: 11-533685-ACAGGAGGCCCCTGCCTGGACG-A
• MyVariant Identifiers: chr11:g.533686_533706del (hg19) ; chr11:g.533686_533706del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533689_533709del , CM000673.2:g.533689_533709del	GRCh38
NC_000011.9:g.533689_533709del , CM000673.1:g.533689_533709del	GRCh37
NC_000011.8:g.523689_523709del	NCBI36
NG_007666.1:g.6845_6865del

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.290+60_291-74del (HRAS)	ENSP00000380722.3:n.290+60_291-74del
ENST00000417302.7:c.290+60_291-74del (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.290+60_291-74del
ENST00000397594.6:c.8+60_9-74del (HRAS)	ENSP00000380722.2:n.8+60_9-74del
ENST00000417302.6:c.290+60_291-74del (HRAS)	ENSP00000388246.1:n.290+60_291-74del
ENST00000462734.2:c.290+60_291-74del (HRAS)	ENSP00000507303.1:n.290+60_291-74del
ENST00000311189.8:c.290+60_291-74del (HRAS) MANE Select	ENSP00000309845.7:n.290+60_291-74del
ENST00000311189.7:c.290+60_291-74del (HRAS)	ENSP00000309845.7:n.290+60_291-74del
ENST00000397594.5:c.290+60_291-74del (HRAS)	ENSP00000380722.1:n.290+60_291-74del
ENST00000397596.6:c.290+60_291-74del (HRAS)	ENSP00000380723.2:n.290+60_291-74del
ENST00000417302.5:c.290+60_291-74del (HRAS)	ENSP00000388246.1:n.290+60_291-74del
ENST00000451590.5:c.290+60_291-74del (HRAS)	ENSP00000407586.1:n.290+60_291-74del
ENST00000479482.1:n.211+60_212-74del (HRAS)
ENST00000493230.5:c.290+60_291-74del (HRAS)	ENSP00000434023.1:n.290+60_291-74del
NM_001130442.1:c.290+60_291-74del (HRAS)	NP_001123914.1:n.290+60_291-74del
NM_005343.2:c.290+60_291-74del (HRAS)	NP_005334.1:n.290+60_291-74del
NM_176795.3:c.290+60_291-74del (HRAS)	NP_789765.1:n.290+60_291-74del
XM_011519875.1:c.-424-4909_-424-4889del (LRRC56)	XP_011518177.1:n.-424-4909_-424-4889del
XM_011519877.1:c.-162+5352_-162+5372del (LRRC56)	XP_011518179.1:n.-162+5352_-162+5372del
XR_242795.1:n.489+60_490-74del (HRAS)
NM_001130442.2:c.290+60_291-74del (HRAS)	NP_001123914.1:n.290+60_291-74del
NM_001318054.1:c.-30+60_-29-74del (HRAS)	NP_001304983.1:n.-30+60_-29-74del
NM_005343.3:c.290+60_291-74del (HRAS)	NP_005334.1:n.290+60_291-74del
NM_176795.4:c.290+60_291-74del (HRAS)	NP_789765.1:n.290+60_291-74del
XM_011519875.2:c.-424-4909_-424-4889del (LRRC56)	XP_011518177.1:n.-424-4909_-424-4889del
XM_011519877.2:c.-162+5352_-162+5372del (LRRC56)	XP_011518179.1:n.-162+5352_-162+5372del
XM_017017167.1:c.-499-4834_-499-4814del (LRRC56)	XP_016872656.1:n.-499-4834_-499-4814del
XM_017017168.1:c.-499-4834_-499-4814del (LRRC56)	XP_016872657.1:n.-499-4834_-499-4814del
NM_005343.4:c.290+60_291-74del (HRAS) MANE Select	NP_005334.1:n.290+60_291-74del
NM_001318054.2:c.-30+60_-29-74del (HRAS)	NP_001304983.1:n.-30+60_-29-74del
NM_001130442.3:c.290+60_291-74del (HRAS)	NP_001123914.1:n.290+60_291-74del
NM_176795.5:c.290+60_291-74del (HRAS) MANE Plus Clinical	NP_789765.1:n.290+60_291-74del