Canonical Allele Identifier: CA2677797922
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945594_29945685del , CM000668.2:g.29945594_29945685del GRCh38
NC_000006.11:g.29913371_29913462del , CM000668.1:g.29913371_29913462del GRCh37
NC_000006.10:g.30021350_30021441del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.1120_1211del ENSP00000492789.2:n.1120_1211del
ENST00000706892.1:n.2946_3037del
ENST00000706893.1:c.*221_*312del ENSP00000516609.1:n.*221_*312del
ENST00000706894.1:c.*221_*312del ENSP00000516610.1:n.*221_*312del
ENST00000706895.1:n.2226_2317del
ENST00000706896.1:n.2533_2624del
ENST00000706897.1:n.1955_2046del
ENST00000706898.1:c.*139_*230del ENSP00000516611.1:n.*139_*230del
ENST00000706899.1:n.2091_2182del
ENST00000706900.1:c.*139_*230del ENSP00000516617.1:n.*139_*230del
ENST00000706901.1:c.*139_*230del ENSP00000516612.1:n.*139_*230del
ENST00000706902.1:c.1093+313_1093+404del ENSP00000516613.1:n.1093+313_1093+404del
ENST00000706903.1:c.*124+15_*124+106del ENSP00000516614.1:n.*124+15_*124+106del
ENST00000706904.1:c.1093+313_1093+404del ENSP00000516615.1:n.1093+313_1093+404del
ENST00000706905.1:c.*139_*230del ENSP00000516616.1:n.*139_*230del
ENST00000376809.10:c.*139_*230del MANE Select ENSP00000366005.5:n.*139_*230del
ENST00000376802.2:c.*139_*230del ENSP00000365998.2:n.*139_*230del
ENST00000376806.9:c.*139_*230del ENSP00000366002.5:n.*139_*230del
ENST00000376809.9:c.*139_*230del ENSP00000366005.5:n.*139_*230del
ENST00000396634.5:c.*139_*230del ENSP00000379873.1:n.*139_*230del
ENST00000495183.5:n.1476_1567del
ENST00000496081.5:n.1496_1587del
NM_002116.7:c.*139_*230del NP_002107.3:n.*139_*230del
NM_002116.8:c.*139_*230del MANE Select NP_002107.3:n.*139_*230del