Canonical Allele Identifier: CA2677797772

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945549-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945549C>G , CM000668.2:g.29945549C>G	GRCh38
NC_000006.11:g.29913326C>G , CM000668.1:g.29913326C>G	GRCh37
NC_000006.10:g.30021305C>G	NCBI36
NG_029217.2:g.8085C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1075C>G	ENSP00000492789.2:n.1075C>G
ENST00000706892.1:n.2901C>G
ENST00000706893.1:c.*176C>G	ENSP00000516609.1:n.*176C>G
ENST00000706894.1:c.*176C>G	ENSP00000516610.1:n.*176C>G
ENST00000706895.1:n.2181C>G
ENST00000706896.1:n.2488C>G
ENST00000706897.1:n.1910C>G
ENST00000706898.1:c.*94C>G	ENSP00000516611.1:n.*94C>G
ENST00000706899.1:n.2046C>G
ENST00000706900.1:c.*94C>G	ENSP00000516617.1:n.*94C>G
ENST00000706901.1:c.*94C>G	ENSP00000516612.1:n.*94C>G
ENST00000706902.1:c.1093+268C>G	ENSP00000516613.1:n.1093+268C>G
ENST00000706903.1:c.*94C>G	ENSP00000516614.1:n.*94C>G
ENST00000706904.1:c.1093+268C>G	ENSP00000516615.1:n.1093+268C>G
ENST00000706905.1:c.*94C>G	ENSP00000516616.1:n.*94C>G
ENST00000376809.10:c.*94C>G MANE Select	ENSP00000366005.5:n.*94C>G
ENST00000376802.2:c.*94C>G	ENSP00000365998.2:n.*94C>G
ENST00000376806.9:c.*94C>G	ENSP00000366002.5:n.*94C>G
ENST00000376809.9:c.*94C>G	ENSP00000366005.5:n.*94C>G
ENST00000396634.5:c.*94C>G	ENSP00000379873.1:n.*94C>G
ENST00000495183.5:n.1431C>G
ENST00000496081.5:n.1451C>G
NM_002116.7:c.*94C>G	NP_002107.3:n.*94C>G
NM_002116.8:c.*94C>G MANE Select	NP_002107.3:n.*94C>G