Canonical Allele Identifier: CA136025780
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs879488407

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945414del , CM000668.2:g.29945414del GRCh38
NC_000006.11:g.29913191del , CM000668.1:g.29913191del GRCh37
NC_000006.10:g.30021170del NCBI36
NG_029217.2:g.7950del

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.977-37del ENSP00000492789.2:n.977-37del
ENST00000706892.1:n.2766del
ENST00000706893.1:c.*78-37del ENSP00000516609.1:n.*78-37del
ENST00000706894.1:c.*41del ENSP00000516610.1:n.*41del
ENST00000706895.1:n.2046del
ENST00000706896.1:n.2390-37del
ENST00000706897.1:n.1812-37del
ENST00000706898.1:c.1112-37del ENSP00000516611.1:n.1112-37del
ENST00000706899.1:n.1948-37del
ENST00000706900.1:c.1010-37del ENSP00000516617.1:n.1010-37del
ENST00000706901.1:c.1094-37del ENSP00000516612.1:n.1094-37del
ENST00000706902.1:c.1093+133del ENSP00000516613.1:n.1093+133del
ENST00000706903.1:c.1094-37del ENSP00000516614.1:n.1094-37del
ENST00000706904.1:c.1093+133del ENSP00000516615.1:n.1093+133del
ENST00000706905.1:c.1094-37del ENSP00000516616.1:n.1094-37del
ENST00000376809.10:c.1094-37del MANE Select ENSP00000366005.5:n.1094-37del
ENST00000376802.2:c.896-37del ENSP00000365998.2:n.896-37del
ENST00000376806.9:c.1112-37del ENSP00000366002.5:n.1112-37del
ENST00000376809.9:c.1094-37del ENSP00000366005.5:n.1094-37del
ENST00000396634.5:c.1094-37del ENSP00000379873.1:n.1094-37del
ENST00000495183.5:n.1333-37del
ENST00000496081.5:n.1353-37del
NM_002116.7:c.1094-37del NP_002107.3:n.1094-37del
NM_002116.8:c.1094-37del MANE Select NP_002107.3:n.1094-37del