Canonical Allele Identifier: CA2677797393
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945454del , CM000668.2:g.29945454del GRCh38
NC_000006.11:g.29913231del , CM000668.1:g.29913231del GRCh37
NC_000006.10:g.30021210del NCBI36
NG_029217.2:g.7990del

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.980del ENSP00000492789.2:p.Ter327=
ENST00000706892.1:n.2806del
ENST00000706893.1:c.*81del ENSP00000516609.1:n.*81del
ENST00000706894.1:c.*81del ENSP00000516610.1:n.*81del
ENST00000706895.1:n.2086del
ENST00000706896.1:n.2393del
ENST00000706897.1:n.1815del
ENST00000706898.1:c.1115del ENSP00000516611.1:p.Ter372=
ENST00000706899.1:n.1951del
ENST00000706900.1:c.1013del ENSP00000516617.1:p.Ter338=
ENST00000706901.1:c.1097del ENSP00000516612.1:p.Ter366=
ENST00000706902.1:c.1093+173del ENSP00000516613.1:n.1093+173del
ENST00000706903.1:c.1097del ENSP00000516614.1:p.Ter366=
ENST00000706904.1:c.1093+173del ENSP00000516615.1:n.1093+173del
ENST00000706905.1:c.1097del ENSP00000516616.1:p.Ter366=
ENST00000376809.10:c.1097del MANE Select ENSP00000366005.5:p.Ter366=
ENST00000376802.2:c.899del ENSP00000365998.2:p.Ter300=
ENST00000376806.9:c.1115del ENSP00000366002.5:p.Ter372=
ENST00000376809.9:c.1097del ENSP00000366005.5:p.Ter366=
ENST00000396634.5:c.1097del ENSP00000379873.1:p.Ter366=
ENST00000495183.5:n.1336del
ENST00000496081.5:n.1356del
NM_002116.7:c.1097del NP_002107.3:p.Ter366=
NM_002116.8:c.1097del MANE Select NP_002107.3:p.Ter366=