Canonical Allele Identifier: CA1947153840

Gene: HRAS LRRC56

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534403_534415delinsGCCCAGGCCCAGC , CM000673.2:g.534403_534415delinsGCCCAGGCCCAGC	GRCh38
NC_000011.9:g.534403_534415delinsGCCCAGGCCCAGC , CM000673.1:g.534403_534415delinsGCCCAGGCCCAGC	GRCh37
NC_000011.8:g.524403_524415delinsGCCCAGGCCCAGC	NCBI36
NG_007666.1:g.6136_6148delinsGCTGGGCCTGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417302.7:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
ENST00000417302.6:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	ENSP00000388246.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
ENST00000462734.2:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	ENSP00000507303.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
ENST00000311189.8:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS) MANE Select	ENSP00000309845.7:n.-53-40_-53-28delinsGCTGGGCCTGGGC
ENST00000311189.7:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	ENSP00000309845.7:n.-53-40_-53-28delinsGCTGGGCCTGGGC
ENST00000397596.6:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	ENSP00000380723.2:n.-53-40_-53-28delinsGCTGGGCCTGGGC
ENST00000417302.5:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	ENSP00000388246.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
ENST00000451590.5:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	ENSP00000407586.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
ENST00000468682.2:n.436-40_436-28delinsGCTGGGCCTGGGC (HRAS)
ENST00000482021.1:n.71-40_71-28delinsGCTGGGCCTGGGC (HRAS)
ENST00000493230.5:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	ENSP00000434023.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
NM_001130442.1:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	NP_001123914.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
NM_005343.2:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	NP_005334.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
NM_176795.3:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	NP_789765.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
XM_011519875.1:c.-424-4195_-424-4183delinsGCCCAGGCCCAGC (LRRC56)	XP_011518177.1:n.-424-4195_-424-4183delinsGCCCAGGCCCAGC
XM_011519877.1:c.-161-5177_-161-5165delinsGCCCAGGCCCAGC (LRRC56)	XP_011518179.1:n.-161-5177_-161-5165delinsGCCCAGGCCCAGC
XR_242795.1:n.147-40_147-28delinsGCTGGGCCTGGGC (HRAS)
NM_001130442.2:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	NP_001123914.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
NM_001318054.1:c.-372-40_-372-28delinsGCTGGGCCTGGGC (HRAS)	NP_001304983.1:n.-372-40_-372-28delinsGCTGGGCCTGGGC
NM_005343.3:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	NP_005334.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
NM_176795.4:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	NP_789765.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
XM_011519875.2:c.-424-4195_-424-4183delinsGCCCAGGCCCAGC (LRRC56)	XP_011518177.1:n.-424-4195_-424-4183delinsGCCCAGGCCCAGC
XM_011519877.2:c.-161-5177_-161-5165delinsGCCCAGGCCCAGC (LRRC56)	XP_011518179.1:n.-161-5177_-161-5165delinsGCCCAGGCCCAGC
XM_017017167.1:c.-499-4120_-499-4108delinsGCCCAGGCCCAGC (LRRC56)	XP_016872656.1:n.-499-4120_-499-4108delinsGCCCAGGCCCAGC
XM_017017168.1:c.-499-4120_-499-4108delinsGCCCAGGCCCAGC (LRRC56)	XP_016872657.1:n.-499-4120_-499-4108delinsGCCCAGGCCCAGC
NM_005343.4:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS) MANE Select	NP_005334.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
NM_001318054.2:c.-372-40_-372-28delinsGCTGGGCCTGGGC (HRAS)	NP_001304983.1:n.-372-40_-372-28delinsGCTGGGCCTGGGC
NM_001130442.3:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS)	NP_001123914.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC
NM_176795.5:c.-53-40_-53-28delinsGCTGGGCCTGGGC (HRAS) MANE Plus Clinical	NP_789765.1:n.-53-40_-53-28delinsGCTGGGCCTGGGC