Canonical Allele Identifier: CA915948742

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 690298
• ClinVar RCV Id: RCV000860022
• dbSNP Id: rs1589792836

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533879_533884delinsAACATCCAGGAC , CM000673.2:g.533879_533884delinsAACATCCAGGAC	GRCh38
NC_000011.9:g.533879_533884delinsAACATCCAGGAC , CM000673.1:g.533879_533884delinsAACATCCAGGAC	GRCh37
NC_000011.8:g.523879_523884delinsAACATCCAGGAC	NCBI36
NG_007666.1:g.6667_6672delinsGTCCTGGATGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.172_177delinsGTCCTGGATGTT (HRAS)	ENSP00000380722.3:p.Thr58_Ala59delinsValLeuAspVal
ENST00000417302.7:c.172_177delinsGTCCTGGATGTT (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Thr58_Ala59delinsValLeuAspVal
ENST00000417302.6:c.172_177delinsGTCCTGGATGTT (HRAS)	ENSP00000388246.1:p.Thr58_Ala59delinsValLeuAspVal
ENST00000462734.2:c.172_177delinsGTCCTGGATGTT (HRAS)	ENSP00000507303.1:p.Thr58_Ala59delinsValLeuAspVal
ENST00000311189.8:c.172_177delinsGTCCTGGATGTT (HRAS) MANE Select	ENSP00000309845.7:p.Thr58_Ala59delinsValLeuAspVal
ENST00000311189.7:c.172_177delinsGTCCTGGATGTT (HRAS)	ENSP00000309845.7:p.Thr58_Ala59delinsValLeuAspVal
ENST00000397594.5:c.172_177delinsGTCCTGGATGTT (HRAS)	ENSP00000380722.1:p.Thr58_Ala59delinsValLeuAspVal
ENST00000397596.6:c.172_177delinsGTCCTGGATGTT (HRAS)	ENSP00000380723.2:p.Thr58_Ala59delinsValLeuAspVal
ENST00000417302.5:c.172_177delinsGTCCTGGATGTT (HRAS)	ENSP00000388246.1:p.Thr58_Ala59delinsValLeuAspVal
ENST00000451590.5:c.172_177delinsGTCCTGGATGTT (HRAS)	ENSP00000407586.1:p.Thr58_Ala59delinsValLeuAspVal
ENST00000468682.2:n.660_665delinsGTCCTGGATGTT (HRAS)
ENST00000479482.1:n.93_98delinsGTCCTGGATGTT (HRAS)
ENST00000493230.5:c.172_177delinsGTCCTGGATGTT (HRAS)	ENSP00000434023.1:p.Thr58_Ala59delinsValLeuAspVal
NM_001130442.1:c.172_177delinsGTCCTGGATGTT (HRAS)	NP_001123914.1:p.Thr58_Ala59delinsValLeuAspVal
NM_005343.2:c.172_177delinsGTCCTGGATGTT (HRAS)	NP_005334.1:p.Thr58_Ala59delinsValLeuAspVal
NM_176795.3:c.172_177delinsGTCCTGGATGTT (HRAS)	NP_789765.1:p.Thr58_Ala59delinsValLeuAspVal
XM_011519875.1:c.-424-4719_-424-4714delinsAACATCCAGGAC (LRRC56)	XP_011518177.1:n.-424-4719_-424-4714delinsAACATCCAGGAC
XM_011519877.1:c.-162+5542_-162+5547delinsAACATCCAGGAC (LRRC56)	XP_011518179.1:n.-162+5542_-162+5547delinsAACATCCAGGAC
XR_242795.1:n.371_376delinsGTCCTGGATGTT (HRAS)
NM_001130442.2:c.172_177delinsGTCCTGGATGTT (HRAS)	NP_001123914.1:p.Thr58_Ala59delinsValLeuAspVal
NM_001318054.1:c.-148_-143delinsGTCCTGGATGTT (HRAS)	NP_001304983.1:n.-148_-143delinsGTCCTGGATGTT
NM_005343.3:c.172_177delinsGTCCTGGATGTT (HRAS)	NP_005334.1:p.Thr58_Ala59delinsValLeuAspVal
NM_176795.4:c.172_177delinsGTCCTGGATGTT (HRAS)	NP_789765.1:p.Thr58_Ala59delinsValLeuAspVal
XM_011519875.2:c.-424-4719_-424-4714delinsAACATCCAGGAC (LRRC56)	XP_011518177.1:n.-424-4719_-424-4714delinsAACATCCAGGAC
XM_011519877.2:c.-162+5542_-162+5547delinsAACATCCAGGAC (LRRC56)	XP_011518179.1:n.-162+5542_-162+5547delinsAACATCCAGGAC
XM_017017167.1:c.-499-4644_-499-4639delinsAACATCCAGGAC (LRRC56)	XP_016872656.1:n.-499-4644_-499-4639delinsAACATCCAGGAC
XM_017017168.1:c.-499-4644_-499-4639delinsAACATCCAGGAC (LRRC56)	XP_016872657.1:n.-499-4644_-499-4639delinsAACATCCAGGAC
NM_005343.4:c.172_177delinsGTCCTGGATGTT (HRAS) MANE Select	NP_005334.1:p.Thr58_Ala59delinsValLeuAspVal
NM_001318054.2:c.-148_-143delinsGTCCTGGATGTT (HRAS)	NP_001304983.1:n.-148_-143delinsGTCCTGGATGTT
NM_001130442.3:c.172_177delinsGTCCTGGATGTT (HRAS)	NP_001123914.1:p.Thr58_Ala59delinsValLeuAspVal
NM_176795.5:c.172_177delinsGTCCTGGATGTT (HRAS) MANE Plus Clinical	NP_789765.1:p.Thr58_Ala59delinsValLeuAspVal