Canonical Allele Identifier: CA1618520720
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945445C= , CM000668.2:g.29945445C= GRCh38
NC_000006.11:g.29913222C= , CM000668.1:g.29913222C= GRCh37
NC_000006.10:g.30021201C= NCBI36
NG_029217.2:g.7981C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.977-6C= ENSP00000492789.2:n.977-6C=
ENST00000706892.1:n.2797C=
ENST00000706893.1:c.*78-6C= ENSP00000516609.1:n.*78-6C=
ENST00000706894.1:c.*72C= ENSP00000516610.1:n.*72C=
ENST00000706895.1:n.2077C=
ENST00000706896.1:n.2390-6C=
ENST00000706897.1:n.1812-6C=
ENST00000706898.1:c.1112-6C= ENSP00000516611.1:n.1112-6C=
ENST00000706899.1:n.1948-6C=
ENST00000706900.1:c.1010-6C= ENSP00000516617.1:n.1010-6C=
ENST00000706901.1:c.1094-6C= ENSP00000516612.1:n.1094-6C=
ENST00000706902.1:c.1093+164C= ENSP00000516613.1:n.1093+164C=
ENST00000706903.1:c.1094-6C= ENSP00000516614.1:n.1094-6C=
ENST00000706904.1:c.1093+164C= ENSP00000516615.1:n.1093+164C=
ENST00000706905.1:c.1094-6C= ENSP00000516616.1:n.1094-6C=
ENST00000376809.10:c.1094-6C= MANE Select ENSP00000366005.5:n.1094-6C=
ENST00000376802.2:c.896-6C= ENSP00000365998.2:n.896-6C=
ENST00000376806.9:c.1112-6C= ENSP00000366002.5:n.1112-6C=
ENST00000376809.9:c.1094-6C= ENSP00000366005.5:n.1094-6C=
ENST00000396634.5:c.1094-6C= ENSP00000379873.1:n.1094-6C=
ENST00000495183.5:n.1333-6C=
ENST00000496081.5:n.1353-6C=
NM_002116.7:c.1094-6C= NP_002107.3:n.1094-6C=
NM_002116.8:c.1094-6C= MANE Select NP_002107.3:n.1094-6C=