Canonical Allele Identifier: CA650546382
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945707dup , CM000668.2:g.29945707dup GRCh38
NC_000006.11:g.29913484dup , CM000668.1:g.29913484dup GRCh37
NC_000006.10:g.30021463dup NCBI36
NG_029217.2:g.8243dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.1233dup ENSP00000492789.2:n.1233dup
ENST00000706893.1:c.*334dup ENSP00000516609.1:n.*334dup
ENST00000706894.1:c.*334dup ENSP00000516610.1:n.*334dup
ENST00000706895.1:n.2339dup
ENST00000706896.1:n.2646dup
ENST00000706897.1:n.2068dup
ENST00000706898.1:c.*252dup ENSP00000516611.1:n.*252dup
ENST00000706899.1:n.2204dup
ENST00000706900.1:c.*252dup ENSP00000516617.1:n.*252dup
ENST00000706901.1:c.*252dup ENSP00000516612.1:n.*252dup
ENST00000706902.1:c.1093+426dup ENSP00000516613.1:n.1093+426dup
ENST00000706903.1:c.*124+128dup ENSP00000516614.1:n.*124+128dup
ENST00000706904.1:c.1093+426dup ENSP00000516615.1:n.1093+426dup
ENST00000706905.1:c.*252dup ENSP00000516616.1:n.*252dup
ENST00000376809.10:c.*252dup MANE Select ENSP00000366005.5:n.*252dup
ENST00000376802.2:c.*252dup ENSP00000365998.2:n.*252dup
ENST00000376806.9:c.*252dup ENSP00000366002.5:n.*252dup
ENST00000376809.9:c.*252dup ENSP00000366005.5:n.*252dup
ENST00000396634.5:c.*252dup ENSP00000379873.1:n.*252dup
ENST00000495183.5:n.1589dup
ENST00000496081.5:n.1609dup
NM_002116.7:c.*252dup NP_002107.3:n.*252dup
NM_002116.8:c.*252dup MANE Select NP_002107.3:n.*252dup