Canonical Allele Identifier: CA2677798433

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945747-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945747C>A , CM000668.2:g.29945747C>A	GRCh38
NC_000006.11:g.29913524C>A , CM000668.1:g.29913524C>A	GRCh37
NC_000006.10:g.30021503C>A	NCBI36
NG_029217.2:g.8283C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.1273C>A	ENSP00000492789.2:n.1273C>A
ENST00000706894.1:c.*374C>A	ENSP00000516610.1:n.*374C>A
ENST00000706895.1:n.2379C>A
ENST00000706896.1:n.2686C>A
ENST00000706897.1:n.2108C>A
ENST00000706898.1:c.*292C>A	ENSP00000516611.1:n.*292C>A
ENST00000706899.1:n.2244C>A
ENST00000706900.1:c.*292C>A	ENSP00000516617.1:n.*292C>A
ENST00000706901.1:c.*292C>A	ENSP00000516612.1:n.*292C>A
ENST00000706902.1:c.1093+466C>A	ENSP00000516613.1:n.1093+466C>A
ENST00000706903.1:c.*124+168C>A	ENSP00000516614.1:n.*124+168C>A
ENST00000706904.1:c.1093+466C>A	ENSP00000516615.1:n.1093+466C>A
ENST00000706905.1:c.*292C>A	ENSP00000516616.1:n.*292C>A
ENST00000376809.10:c.*292C>A MANE Select	ENSP00000366005.5:n.*292C>A
ENST00000376802.2:c.*292C>A	ENSP00000365998.2:n.*292C>A
ENST00000376806.9:c.*292C>A	ENSP00000366002.5:n.*292C>A
ENST00000376809.9:c.*292C>A	ENSP00000366005.5:n.*292C>A
ENST00000396634.5:c.*292C>A	ENSP00000379873.1:n.*292C>A
ENST00000495183.5:n.1629C>A
ENST00000496081.5:n.1649C>A
NM_002116.7:c.*292C>A	NP_002107.3:n.*292C>A
NM_002116.8:c.*292C>A MANE Select	NP_002107.3:n.*292C>A