Canonical Allele Identifier: CA2770464040

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945832C>T , CM000668.2:g.29945832C>T	GRCh38
NC_000006.11:g.29913609C>T , CM000668.1:g.29913609C>T	GRCh37
NC_000006.10:g.30021588C>T	NCBI36
NG_029217.2:g.8368C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1358C>T	ENSP00000492789.2:n.1358C>T
ENST00000706896.1:n.2771C>T
ENST00000706897.1:n.2193C>T
ENST00000706898.1:c.*377C>T	ENSP00000516611.1:n.*377C>T
ENST00000706899.1:n.2329C>T
ENST00000706900.1:c.*377C>T	ENSP00000516617.1:n.*377C>T
ENST00000706901.1:c.*377C>T	ENSP00000516612.1:n.*377C>T
ENST00000706902.1:c.1093+551C>T	ENSP00000516613.1:n.1093+551C>T
ENST00000706903.1:c.*124+253C>T	ENSP00000516614.1:n.*124+253C>T
ENST00000706904.1:c.1093+551C>T	ENSP00000516615.1:n.1093+551C>T
ENST00000706905.1:c.*377C>T	ENSP00000516616.1:n.*377C>T
ENST00000376809.10:c.*377C>T MANE Select	ENSP00000366005.5:n.*377C>T
ENST00000376802.2:c.*377C>T	ENSP00000365998.2:n.*377C>T
ENST00000376806.9:c.*377C>T	ENSP00000366002.5:n.*377C>T
ENST00000376809.9:c.*377C>T	ENSP00000366005.5:n.*377C>T
ENST00000396634.5:c.*377C>T	ENSP00000379873.1:n.*377C>T
ENST00000495183.5:n.1714C>T
ENST00000496081.5:n.1734C>T
NM_002116.7:c.*377C>T	NP_002107.3:n.*377C>T
NM_002116.8:c.*377C>T MANE Select	NP_002107.3:n.*377C>T