Canonical Allele Identifier: CA2677798642

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945794-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945794C>A , CM000668.2:g.29945794C>A	GRCh38
NC_000006.11:g.29913571C>A , CM000668.1:g.29913571C>A	GRCh37
NC_000006.10:g.30021550C>A	NCBI36
NG_029217.2:g.8330C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1320C>A	ENSP00000492789.2:n.1320C>A
ENST00000706896.1:n.2733C>A
ENST00000706897.1:n.2155C>A
ENST00000706898.1:c.*339C>A	ENSP00000516611.1:n.*339C>A
ENST00000706899.1:n.2291C>A
ENST00000706900.1:c.*339C>A	ENSP00000516617.1:n.*339C>A
ENST00000706901.1:c.*339C>A	ENSP00000516612.1:n.*339C>A
ENST00000706902.1:c.1093+513C>A	ENSP00000516613.1:n.1093+513C>A
ENST00000706903.1:c.*124+215C>A	ENSP00000516614.1:n.*124+215C>A
ENST00000706904.1:c.1093+513C>A	ENSP00000516615.1:n.1093+513C>A
ENST00000706905.1:c.*339C>A	ENSP00000516616.1:n.*339C>A
ENST00000376809.10:c.*339C>A MANE Select	ENSP00000366005.5:n.*339C>A
ENST00000376802.2:c.*339C>A	ENSP00000365998.2:n.*339C>A
ENST00000376806.9:c.*339C>A	ENSP00000366002.5:n.*339C>A
ENST00000376809.9:c.*339C>A	ENSP00000366005.5:n.*339C>A
ENST00000396634.5:c.*339C>A	ENSP00000379873.1:n.*339C>A
ENST00000495183.5:n.1676C>A
ENST00000496081.5:n.1696C>A
NM_002116.7:c.*339C>A	NP_002107.3:n.*339C>A
NM_002116.8:c.*339C>A MANE Select	NP_002107.3:n.*339C>A