Canonical Allele Identifier: CA650546351
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945568dup , CM000668.2:g.29945568dup GRCh38
NC_000006.11:g.29913345dup , CM000668.1:g.29913345dup GRCh37
NC_000006.10:g.30021324dup NCBI36
NG_029217.2:g.8104dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.1094dup ENSP00000492789.2:n.1094dup
ENST00000706892.1:n.2920dup
ENST00000706893.1:c.*195dup ENSP00000516609.1:n.*195dup
ENST00000706894.1:c.*195dup ENSP00000516610.1:n.*195dup
ENST00000706895.1:n.2200dup
ENST00000706896.1:n.2507dup
ENST00000706897.1:n.1929dup
ENST00000706898.1:c.*113dup ENSP00000516611.1:n.*113dup
ENST00000706899.1:n.2065dup
ENST00000706900.1:c.*113dup ENSP00000516617.1:n.*113dup
ENST00000706901.1:c.*113dup ENSP00000516612.1:n.*113dup
ENST00000706902.1:c.1093+287dup ENSP00000516613.1:n.1093+287dup
ENST00000706903.1:c.*113dup ENSP00000516614.1:n.*113dup
ENST00000706904.1:c.1093+287dup ENSP00000516615.1:n.1093+287dup
ENST00000706905.1:c.*113dup ENSP00000516616.1:n.*113dup
ENST00000376809.10:c.*113dup MANE Select ENSP00000366005.5:n.*113dup
ENST00000376802.2:c.*113dup ENSP00000365998.2:n.*113dup
ENST00000376806.9:c.*113dup ENSP00000366002.5:n.*113dup
ENST00000376809.9:c.*113dup ENSP00000366005.5:n.*113dup
ENST00000396634.5:c.*113dup ENSP00000379873.1:n.*113dup
ENST00000495183.5:n.1450dup
ENST00000496081.5:n.1470dup
NM_002116.7:c.*113dup NP_002107.3:n.*113dup
NM_002116.8:c.*113dup MANE Select NP_002107.3:n.*113dup