Canonical Allele Identifier: CA2677798814

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945853-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945853A>G , CM000668.2:g.29945853A>G	GRCh38
NC_000006.11:g.29913630A>G , CM000668.1:g.29913630A>G	GRCh37
NC_000006.10:g.30021609A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1379A>G	ENSP00000492789.2:n.1379A>G
ENST00000706899.1:n.2350A>G
ENST00000706900.1:c.*398A>G	ENSP00000516617.1:n.*398A>G
ENST00000706901.1:c.*398A>G	ENSP00000516612.1:n.*398A>G
ENST00000706902.1:c.1093+572A>G	ENSP00000516613.1:n.1093+572A>G
ENST00000706903.1:c.*124+274A>G	ENSP00000516614.1:n.*124+274A>G
ENST00000706904.1:c.1093+572A>G	ENSP00000516615.1:n.1093+572A>G
ENST00000706905.1:c.*398A>G	ENSP00000516616.1:n.*398A>G
ENST00000376809.10:c.*398A>G MANE Select	ENSP00000366005.5:n.*398A>G
ENST00000376802.2:c.*398A>G	ENSP00000365998.2:n.*398A>G
ENST00000376806.9:c.*398A>G	ENSP00000366002.5:n.*398A>G
ENST00000376809.9:c.*398A>G	ENSP00000366005.5:n.*398A>G
ENST00000396634.5:c.*398A>G	ENSP00000379873.1:n.*398A>G
ENST00000495183.5:n.1735A>G
ENST00000496081.5:n.1755A>G
NM_002116.7:c.*398A>G	NP_002107.3:n.*398A>G
NM_002116.8:c.*398A>G MANE Select	NP_002107.3:n.*398A>G