Canonical Allele Identifier: CA2536493256

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945313G>C , CM000668.2:g.29945313G>C	GRCh38
NC_000006.11:g.29913090G>C , CM000668.1:g.29913090G>C	GRCh37
NC_000006.10:g.30021069G>C	NCBI36
NG_029217.2:g.7849G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.976+32G>C	ENSP00000492789.2:n.976+32G>C
ENST00000706892.1:n.2665G>C
ENST00000706893.1:c.*77+32G>C	ENSP00000516609.1:n.*77+32G>C
ENST00000706894.1:c.1125G>C	ENSP00000516610.1:p.Gly375=
ENST00000706895.1:n.1945G>C
ENST00000706896.1:n.2389+32G>C
ENST00000706897.1:n.1811+32G>C
ENST00000706898.1:c.1111+32G>C	ENSP00000516611.1:n.1111+32G>C
ENST00000706899.1:n.1947+32G>C
ENST00000706900.1:c.1009+32G>C	ENSP00000516617.1:n.1009+32G>C
ENST00000706901.1:c.1093+32G>C	ENSP00000516612.1:n.1093+32G>C
ENST00000706902.1:c.1093+32G>C	ENSP00000516613.1:n.1093+32G>C
ENST00000706903.1:c.1093+32G>C	ENSP00000516614.1:n.1093+32G>C
ENST00000706904.1:c.1093+32G>C	ENSP00000516615.1:n.1093+32G>C
ENST00000706905.1:c.1093+32G>C	ENSP00000516616.1:n.1093+32G>C
ENST00000376809.10:c.1093+32G>C MANE Select	ENSP00000366005.5:n.1093+32G>C
ENST00000376802.2:c.896-138G>C	ENSP00000365998.2:n.896-138G>C
ENST00000376806.9:c.1111+32G>C	ENSP00000366002.5:n.1111+32G>C
ENST00000376809.9:c.1093+32G>C	ENSP00000366005.5:n.1093+32G>C
ENST00000396634.5:c.1093+32G>C	ENSP00000379873.1:n.1093+32G>C
ENST00000495183.5:n.1332+32G>C
ENST00000496081.5:n.1352+32G>C
NM_002116.7:c.1093+32G>C	NP_002107.3:n.1093+32G>C
NM_002116.8:c.1093+32G>C MANE Select	NP_002107.3:n.1093+32G>C