Canonical Allele Identifier: CA1947153241

Gene: HRAS LRRC56

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533460_533474delinsGTCTTGGCCGAGGTC , CM000673.2:g.533460_533474delinsGTCTTGGCCGAGGTC	GRCh38
NC_000011.9:g.533460_533474delinsGTCTTGGCCGAGGTC , CM000673.1:g.533460_533474delinsGTCTTGGCCGAGGTC	GRCh37
NC_000011.8:g.523460_523474delinsGTCTTGGCCGAGGTC	NCBI36
NG_007666.1:g.7077_7091delinsGACCTCGGCCAAGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	ENSP00000380722.3:p.Glu143=
ENST00000417302.7:c.429_443delinsGACCTCGGCCAAGAC (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Glu143=
ENST00000397594.6:c.147_161delinsGACCTCGGCCAAGAC (HRAS)	ENSP00000380722.2:p.Glu49=
ENST00000417302.6:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	ENSP00000388246.1:p.Glu143=
ENST00000462734.2:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	ENSP00000507303.1:p.Glu143=
ENST00000311189.8:c.429_443delinsGACCTCGGCCAAGAC (HRAS) MANE Select	ENSP00000309845.7:p.Glu143=
ENST00000311189.7:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	ENSP00000309845.7:p.Glu143=
ENST00000397594.5:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	ENSP00000380722.1:p.Glu143=
ENST00000397596.6:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	ENSP00000380723.2:p.Glu143=
ENST00000417302.5:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	ENSP00000388246.1:p.Glu143=
ENST00000451590.5:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	ENSP00000407586.1:p.Glu143=
ENST00000462734.1:n.122_136delinsGACCTCGGCCAAGAC (HRAS)
ENST00000478324.5:n.139_153delinsGACCTCGGCCAAGAC (HRAS)
ENST00000479482.1:n.350_364delinsGACCTCGGCCAAGAC (HRAS)
ENST00000493230.5:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	ENSP00000434023.1:p.Glu143=
NM_001130442.1:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	NP_001123914.1:p.Glu143=
NM_005343.2:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	NP_005334.1:p.Glu143=
NM_176795.3:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	NP_789765.1:p.Glu143=
XM_011519875.1:c.-425+5123_-424-5124delinsGTCTTGGCCGAGGTC (LRRC56)	XP_011518177.1:n.-425+5123_-424-5124delinsGTCTTGGCCGAGGTC
XM_011519877.1:c.-162+5123_-162+5137delinsGTCTTGGCCGAGGTC (LRRC56)	XP_011518179.1:n.-162+5123_-162+5137delinsGTCTTGGCCGAGGTC
XR_242795.1:n.628_642delinsGACCTCGGCCAAGAC (HRAS)
NM_001130442.2:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	NP_001123914.1:p.Glu143=
NM_001318054.1:c.110_124delinsGACCTCGGCCAAGAC (HRAS)	NP_001304983.1:p.Arg37=
NM_005343.3:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	NP_005334.1:p.Glu143=
NM_176795.4:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	NP_789765.1:p.Glu143=
XM_011519875.2:c.-425+5123_-424-5124delinsGTCTTGGCCGAGGTC (LRRC56)	XP_011518177.1:n.-425+5123_-424-5124delinsGTCTTGGCCGAGGTC
XM_011519877.2:c.-162+5123_-162+5137delinsGTCTTGGCCGAGGTC (LRRC56)	XP_011518179.1:n.-162+5123_-162+5137delinsGTCTTGGCCGAGGTC
XM_017017167.1:c.-499-5063_-499-5049delinsGTCTTGGCCGAGGTC (LRRC56)	XP_016872656.1:n.-499-5063_-499-5049delinsGTCTTGGCCGAGGTC
XM_017017168.1:c.-499-5063_-499-5049delinsGTCTTGGCCGAGGTC (LRRC56)	XP_016872657.1:n.-499-5063_-499-5049delinsGTCTTGGCCGAGGTC
NM_005343.4:c.429_443delinsGACCTCGGCCAAGAC (HRAS) MANE Select	NP_005334.1:p.Glu143=
NM_001318054.2:c.110_124delinsGACCTCGGCCAAGAC (HRAS)	NP_001304983.1:p.Arg37=
NM_001130442.3:c.429_443delinsGACCTCGGCCAAGAC (HRAS)	NP_001123914.1:p.Glu143=
NM_176795.5:c.429_443delinsGACCTCGGCCAAGAC (HRAS) MANE Plus Clinical	NP_789765.1:p.Glu143=