Canonical Allele Identifier: CA2677798108

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945673-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945673C>A , CM000668.2:g.29945673C>A	GRCh38
NC_000006.11:g.29913450C>A , CM000668.1:g.29913450C>A	GRCh37
NC_000006.10:g.30021429C>A	NCBI36
NG_029217.2:g.8209C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1199C>A	ENSP00000492789.2:n.1199C>A
ENST00000706892.1:n.3025C>A
ENST00000706893.1:c.*300C>A	ENSP00000516609.1:n.*300C>A
ENST00000706894.1:c.*300C>A	ENSP00000516610.1:n.*300C>A
ENST00000706895.1:n.2305C>A
ENST00000706896.1:n.2612C>A
ENST00000706897.1:n.2034C>A
ENST00000706898.1:c.*218C>A	ENSP00000516611.1:n.*218C>A
ENST00000706899.1:n.2170C>A
ENST00000706900.1:c.*218C>A	ENSP00000516617.1:n.*218C>A
ENST00000706901.1:c.*218C>A	ENSP00000516612.1:n.*218C>A
ENST00000706902.1:c.1093+392C>A	ENSP00000516613.1:n.1093+392C>A
ENST00000706903.1:c.*124+94C>A	ENSP00000516614.1:n.*124+94C>A
ENST00000706904.1:c.1093+392C>A	ENSP00000516615.1:n.1093+392C>A
ENST00000706905.1:c.*218C>A	ENSP00000516616.1:n.*218C>A
ENST00000376809.10:c.*218C>A MANE Select	ENSP00000366005.5:n.*218C>A
ENST00000376802.2:c.*218C>A	ENSP00000365998.2:n.*218C>A
ENST00000376806.9:c.*218C>A	ENSP00000366002.5:n.*218C>A
ENST00000376809.9:c.*218C>A	ENSP00000366005.5:n.*218C>A
ENST00000396634.5:c.*218C>A	ENSP00000379873.1:n.*218C>A
ENST00000495183.5:n.1555C>A
ENST00000496081.5:n.1575C>A
NM_002116.7:c.*218C>A	NP_002107.3:n.*218C>A
NM_002116.8:c.*218C>A MANE Select	NP_002107.3:n.*218C>A