Canonical Allele Identifier: CA823769989

Gene: HLA-A

Linked Data

• dbSNP Id: rs1308070709
• gnomAD v3: 6-29945763-C-G
• gnomAD v4: 6-29945763-C-G
• MyVariant Identifiers: chr6:g.29913540C>G (hg19) ; chr6:g.29945763C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945763C>G , CM000668.2:g.29945763C>G	GRCh38
NC_000006.11:g.29913540C>G , CM000668.1:g.29913540C>G	GRCh37
NC_000006.10:g.30021519C>G	NCBI36
NG_029217.2:g.8299C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1289C>G	ENSP00000492789.2:n.1289C>G
ENST00000706895.1:n.2395C>G
ENST00000706896.1:n.2702C>G
ENST00000706897.1:n.2124C>G
ENST00000706898.1:c.*308C>G	ENSP00000516611.1:n.*308C>G
ENST00000706899.1:n.2260C>G
ENST00000706900.1:c.*308C>G	ENSP00000516617.1:n.*308C>G
ENST00000706901.1:c.*308C>G	ENSP00000516612.1:n.*308C>G
ENST00000706902.1:c.1093+482C>G	ENSP00000516613.1:n.1093+482C>G
ENST00000706903.1:c.*124+184C>G	ENSP00000516614.1:n.*124+184C>G
ENST00000706904.1:c.1093+482C>G	ENSP00000516615.1:n.1093+482C>G
ENST00000706905.1:c.*308C>G	ENSP00000516616.1:n.*308C>G
ENST00000376809.10:c.*308C>G MANE Select	ENSP00000366005.5:n.*308C>G
ENST00000376802.2:c.*308C>G	ENSP00000365998.2:n.*308C>G
ENST00000376806.9:c.*308C>G	ENSP00000366002.5:n.*308C>G
ENST00000376809.9:c.*308C>G	ENSP00000366005.5:n.*308C>G
ENST00000396634.5:c.*308C>G	ENSP00000379873.1:n.*308C>G
ENST00000495183.5:n.1645C>G
ENST00000496081.5:n.1665C>G
NM_002116.7:c.*308C>G	NP_002107.3:n.*308C>G
NM_002116.8:c.*308C>G MANE Select	NP_002107.3:n.*308C>G