Canonical Allele Identifier: CA1087350223
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945415_29945416del , CM000668.2:g.29945415_29945416del GRCh38
NC_000006.11:g.29913192_29913193del , CM000668.1:g.29913192_29913193del GRCh37
NC_000006.10:g.30021171_30021172del NCBI36
NG_029217.2:g.7951_7952del

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.977-36_977-35del ENSP00000492789.2:n.977-36_977-35del
ENST00000706892.1:n.2767_2768del
ENST00000706893.1:c.*78-36_*78-35del ENSP00000516609.1:n.*78-36_*78-35del
ENST00000706894.1:c.*42_*43del ENSP00000516610.1:n.*42_*43del
ENST00000706895.1:n.2047_2048del
ENST00000706896.1:n.2390-36_2390-35del
ENST00000706897.1:n.1812-36_1812-35del
ENST00000706898.1:c.1112-36_1112-35del ENSP00000516611.1:n.1112-36_1112-35del
ENST00000706899.1:n.1948-36_1948-35del
ENST00000706900.1:c.1010-36_1010-35del ENSP00000516617.1:n.1010-36_1010-35del
ENST00000706901.1:c.1094-36_1094-35del ENSP00000516612.1:n.1094-36_1094-35del
ENST00000706902.1:c.1093+134_1093+135del ENSP00000516613.1:n.1093+134_1093+135del
ENST00000706903.1:c.1094-36_1094-35del ENSP00000516614.1:n.1094-36_1094-35del
ENST00000706904.1:c.1093+134_1093+135del ENSP00000516615.1:n.1093+134_1093+135del
ENST00000706905.1:c.1094-36_1094-35del ENSP00000516616.1:n.1094-36_1094-35del
ENST00000376809.10:c.1094-36_1094-35del MANE Select ENSP00000366005.5:n.1094-36_1094-35del
ENST00000376802.2:c.896-36_896-35del ENSP00000365998.2:n.896-36_896-35del
ENST00000376806.9:c.1112-36_1112-35del ENSP00000366002.5:n.1112-36_1112-35del
ENST00000376809.9:c.1094-36_1094-35del ENSP00000366005.5:n.1094-36_1094-35del
ENST00000396634.5:c.1094-36_1094-35del ENSP00000379873.1:n.1094-36_1094-35del
ENST00000495183.5:n.1333-36_1333-35del
ENST00000496081.5:n.1353-36_1353-35del
NM_002116.7:c.1094-36_1094-35del NP_002107.3:n.1094-36_1094-35del
NM_002116.8:c.1094-36_1094-35del MANE Select NP_002107.3:n.1094-36_1094-35del