Canonical Allele Identifier: CA2526104643

Gene: HRAS LRRC56

Linked Data

• gnomAD v4: 11-534410-CCCAGCCCCAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534411_534420del , CM000673.2:g.534411_534420del	GRCh38
NC_000011.9:g.534411_534420del , CM000673.1:g.534411_534420del	GRCh37
NC_000011.8:g.524411_524420del	NCBI36
NG_007666.1:g.6131_6140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417302.7:c.-53-45_-53-36del (HRAS) MANE Plus Clinical	ENSP00000388246.1:n.-53-45_-53-36del
ENST00000417302.6:c.-53-45_-53-36del (HRAS)	ENSP00000388246.1:n.-53-45_-53-36del
ENST00000462734.2:c.-53-45_-53-36del (HRAS)	ENSP00000507303.1:n.-53-45_-53-36del
ENST00000311189.8:c.-53-45_-53-36del (HRAS) MANE Select	ENSP00000309845.7:n.-53-45_-53-36del
ENST00000311189.7:c.-53-45_-53-36del (HRAS)	ENSP00000309845.7:n.-53-45_-53-36del
ENST00000397596.6:c.-53-45_-53-36del (HRAS)	ENSP00000380723.2:n.-53-45_-53-36del
ENST00000417302.5:c.-53-45_-53-36del (HRAS)	ENSP00000388246.1:n.-53-45_-53-36del
ENST00000451590.5:c.-53-45_-53-36del (HRAS)	ENSP00000407586.1:n.-53-45_-53-36del
ENST00000468682.2:n.436-45_436-36del (HRAS)
ENST00000482021.1:n.71-45_71-36del (HRAS)
ENST00000493230.5:c.-53-45_-53-36del (HRAS)	ENSP00000434023.1:n.-53-45_-53-36del
NM_001130442.1:c.-53-45_-53-36del (HRAS)	NP_001123914.1:n.-53-45_-53-36del
NM_005343.2:c.-53-45_-53-36del (HRAS)	NP_005334.1:n.-53-45_-53-36del
NM_176795.3:c.-53-45_-53-36del (HRAS)	NP_789765.1:n.-53-45_-53-36del
XM_011519875.1:c.-424-4187_-424-4178del (LRRC56)	XP_011518177.1:n.-424-4187_-424-4178del
XM_011519877.1:c.-161-5169_-161-5160del (LRRC56)	XP_011518179.1:n.-161-5169_-161-5160del
XR_242795.1:n.147-45_147-36del (HRAS)
NM_001130442.2:c.-53-45_-53-36del (HRAS)	NP_001123914.1:n.-53-45_-53-36del
NM_001318054.1:c.-372-45_-372-36del (HRAS)	NP_001304983.1:n.-372-45_-372-36del
NM_005343.3:c.-53-45_-53-36del (HRAS)	NP_005334.1:n.-53-45_-53-36del
NM_176795.4:c.-53-45_-53-36del (HRAS)	NP_789765.1:n.-53-45_-53-36del
XM_011519875.2:c.-424-4187_-424-4178del (LRRC56)	XP_011518177.1:n.-424-4187_-424-4178del
XM_011519877.2:c.-161-5169_-161-5160del (LRRC56)	XP_011518179.1:n.-161-5169_-161-5160del
XM_017017167.1:c.-499-4112_-499-4103del (LRRC56)	XP_016872656.1:n.-499-4112_-499-4103del
XM_017017168.1:c.-499-4112_-499-4103del (LRRC56)	XP_016872657.1:n.-499-4112_-499-4103del
NM_005343.4:c.-53-45_-53-36del (HRAS) MANE Select	NP_005334.1:n.-53-45_-53-36del
NM_001318054.2:c.-372-45_-372-36del (HRAS)	NP_001304983.1:n.-372-45_-372-36del
NM_001130442.3:c.-53-45_-53-36del (HRAS)	NP_001123914.1:n.-53-45_-53-36del
NM_176795.5:c.-53-45_-53-36del (HRAS) MANE Plus Clinical	NP_789765.1:n.-53-45_-53-36del