Canonical Allele Identifier: CA1618520689
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945428T= , CM000668.2:g.29945428T= GRCh38
NC_000006.11:g.29913205T= , CM000668.1:g.29913205T= GRCh37
NC_000006.10:g.30021184T= NCBI36
NG_029217.2:g.7964T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.977-23T= ENSP00000492789.2:n.977-23T=
ENST00000706892.1:n.2780T=
ENST00000706893.1:c.*78-23T= ENSP00000516609.1:n.*78-23T=
ENST00000706894.1:c.*55T= ENSP00000516610.1:n.*55T=
ENST00000706895.1:n.2060T=
ENST00000706896.1:n.2390-23T=
ENST00000706897.1:n.1812-23T=
ENST00000706898.1:c.1112-23T= ENSP00000516611.1:n.1112-23T=
ENST00000706899.1:n.1948-23T=
ENST00000706900.1:c.1010-23T= ENSP00000516617.1:n.1010-23T=
ENST00000706901.1:c.1094-23T= ENSP00000516612.1:n.1094-23T=
ENST00000706902.1:c.1093+147T= ENSP00000516613.1:n.1093+147T=
ENST00000706903.1:c.1094-23T= ENSP00000516614.1:n.1094-23T=
ENST00000706904.1:c.1093+147T= ENSP00000516615.1:n.1093+147T=
ENST00000706905.1:c.1094-23T= ENSP00000516616.1:n.1094-23T=
ENST00000376809.10:c.1094-23T= MANE Select ENSP00000366005.5:n.1094-23T=
ENST00000376802.2:c.896-23T= ENSP00000365998.2:n.896-23T=
ENST00000376806.9:c.1112-23T= ENSP00000366002.5:n.1112-23T=
ENST00000376809.9:c.1094-23T= ENSP00000366005.5:n.1094-23T=
ENST00000396634.5:c.1094-23T= ENSP00000379873.1:n.1094-23T=
ENST00000495183.5:n.1333-23T=
ENST00000496081.5:n.1353-23T=
NM_002116.7:c.1094-23T= NP_002107.3:n.1094-23T=
NM_002116.8:c.1094-23T= MANE Select NP_002107.3:n.1094-23T=