Canonical Allele Identifier: CA2790128315

Gene: HRAS LRRC56

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533682_533719del , CM000673.2:g.533682_533719del	GRCh38
NC_000011.9:g.533682_533719del , CM000673.1:g.533682_533719del	GRCh37
NC_000011.8:g.523682_523719del	NCBI36
NG_007666.1:g.6832_6869del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.290+47_291-70del (HRAS)	ENSP00000380722.3:n.290+47_291-70del
ENST00000417302.7:c.290+47_291-70del (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.290+47_291-70del
ENST00000397594.6:c.8+47_9-70del (HRAS)	ENSP00000380722.2:n.8+47_9-70del
ENST00000417302.6:c.290+47_291-70del (HRAS)	ENSP00000388246.1:n.290+47_291-70del
ENST00000462734.2:c.290+47_291-70del (HRAS)	ENSP00000507303.1:n.290+47_291-70del
ENST00000311189.8:c.290+47_291-70del (HRAS) MANE Select	ENSP00000309845.7:n.290+47_291-70del
ENST00000311189.7:c.290+47_291-70del (HRAS)	ENSP00000309845.7:n.290+47_291-70del
ENST00000397594.5:c.290+47_291-70del (HRAS)	ENSP00000380722.1:n.290+47_291-70del
ENST00000397596.6:c.290+47_291-70del (HRAS)	ENSP00000380723.2:n.290+47_291-70del
ENST00000417302.5:c.290+47_291-70del (HRAS)	ENSP00000388246.1:n.290+47_291-70del
ENST00000451590.5:c.290+47_291-70del (HRAS)	ENSP00000407586.1:n.290+47_291-70del
ENST00000479482.1:n.211+47_212-70del (HRAS)
ENST00000493230.5:c.290+47_291-70del (HRAS)	ENSP00000434023.1:n.290+47_291-70del
NM_001130442.1:c.290+47_291-70del (HRAS)	NP_001123914.1:n.290+47_291-70del
NM_005343.2:c.290+47_291-70del (HRAS)	NP_005334.1:n.290+47_291-70del
NM_176795.3:c.290+47_291-70del (HRAS)	NP_789765.1:n.290+47_291-70del
XM_011519875.1:c.-424-4916_-424-4879del (LRRC56)	XP_011518177.1:n.-424-4916_-424-4879del
XM_011519877.1:c.-162+5345_-162+5382del (LRRC56)	XP_011518179.1:n.-162+5345_-162+5382del
XR_242795.1:n.489+47_490-70del (HRAS)
NM_001130442.2:c.290+47_291-70del (HRAS)	NP_001123914.1:n.290+47_291-70del
NM_001318054.1:c.-30+47_-29-70del (HRAS)	NP_001304983.1:n.-30+47_-29-70del
NM_005343.3:c.290+47_291-70del (HRAS)	NP_005334.1:n.290+47_291-70del
NM_176795.4:c.290+47_291-70del (HRAS)	NP_789765.1:n.290+47_291-70del
XM_011519875.2:c.-424-4916_-424-4879del (LRRC56)	XP_011518177.1:n.-424-4916_-424-4879del
XM_011519877.2:c.-162+5345_-162+5382del (LRRC56)	XP_011518179.1:n.-162+5345_-162+5382del
XM_017017167.1:c.-499-4841_-499-4804del (LRRC56)	XP_016872656.1:n.-499-4841_-499-4804del
XM_017017168.1:c.-499-4841_-499-4804del (LRRC56)	XP_016872657.1:n.-499-4841_-499-4804del
NM_005343.4:c.290+47_291-70del (HRAS) MANE Select	NP_005334.1:n.290+47_291-70del
NM_001318054.2:c.-30+47_-29-70del (HRAS)	NP_001304983.1:n.-30+47_-29-70del
NM_001130442.3:c.290+47_291-70del (HRAS)	NP_001123914.1:n.290+47_291-70del
NM_176795.5:c.290+47_291-70del (HRAS) MANE Plus Clinical	NP_789765.1:n.290+47_291-70del