Canonical Allele Identifier: CA645569129

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 1390411
• ClinVar RCV Id: RCV001917597
• dbSNP Id: rs2133986181
• COSMIC: COSM1745406 ; COSM1745407

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533460del , CM000673.2:g.533460del	GRCh38
NC_000011.9:g.533460del , CM000673.1:g.533460del	GRCh37
NC_000011.8:g.523460del	NCBI36
NG_007666.1:g.7093del

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.445del (HRAS)	ENSP00000380722.3:p.Arg149GlyfsTer?
ENST00000417302.7:c.445del (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Arg149GlyfsTer?
ENST00000397594.6:c.163del (HRAS)	ENSP00000380722.2:p.Arg55GlyfsTer?
ENST00000417302.6:c.445del (HRAS)	ENSP00000388246.1:p.Arg149GlyfsTer?
ENST00000462734.2:c.445del (HRAS)	ENSP00000507303.1:p.Arg149GlyfsTer21
ENST00000311189.8:c.445del (HRAS) MANE Select	ENSP00000309845.7:p.Arg149GlyfsTer23
ENST00000311189.7:c.445del (HRAS)	ENSP00000309845.7:p.Arg149GlyfsTer23
ENST00000397594.5:c.445del (HRAS)	ENSP00000380722.1:p.Arg149GlyfsTer?
ENST00000397596.6:c.445del (HRAS)	ENSP00000380723.2:p.Arg149GlyfsTer23
ENST00000417302.5:c.445del (HRAS)	ENSP00000388246.1:p.Arg149GlyfsTer?
ENST00000451590.5:c.445del (HRAS)	ENSP00000407586.1:p.Arg149GlyfsTer23
ENST00000462734.1:n.138del (HRAS)
ENST00000478324.5:n.155del (HRAS)
ENST00000479482.1:n.366del (HRAS)
ENST00000493230.5:c.445del (HRAS)	ENSP00000434023.1:p.Arg149GlyfsTer?
NM_001130442.1:c.445del (HRAS)	NP_001123914.1:p.Arg149GlyfsTer23
NM_005343.2:c.445del (HRAS)	NP_005334.1:p.Arg149GlyfsTer23
NM_176795.3:c.445del (HRAS)	NP_789765.1:p.Arg149GlyfsTer?
XM_011519875.1:c.-425+5123del (LRRC56)	XP_011518177.1:n.-425+5123del
XM_011519877.1:c.-162+5123del (LRRC56)	XP_011518179.1:n.-162+5123del
XR_242795.1:n.644del (HRAS)
NM_001130442.2:c.445del (HRAS)	NP_001123914.1:p.Arg149GlyfsTer23
NM_001318054.1:c.126del (HRAS)	NP_001304983.1:p.Gly43AlafsTer8
NM_005343.3:c.445del (HRAS)	NP_005334.1:p.Arg149GlyfsTer23
NM_176795.4:c.445del (HRAS)	NP_789765.1:p.Arg149GlyfsTer?
XM_011519875.2:c.-425+5123del (LRRC56)	XP_011518177.1:n.-425+5123del
XM_011519877.2:c.-162+5123del (LRRC56)	XP_011518179.1:n.-162+5123del
XM_017017167.1:c.-499-5063del (LRRC56)	XP_016872656.1:n.-499-5063del
XM_017017168.1:c.-499-5063del (LRRC56)	XP_016872657.1:n.-499-5063del
NM_005343.4:c.445del (HRAS) MANE Select	NP_005334.1:p.Arg149GlyfsTer23
NM_001318054.2:c.126del (HRAS)	NP_001304983.1:p.Gly43AlafsTer8
NM_001130442.3:c.445del (HRAS)	NP_001123914.1:p.Arg149GlyfsTer23
NM_176795.5:c.445del (HRAS) MANE Plus Clinical	NP_789765.1:p.Arg149GlyfsTer?