Canonical Allele Identifier: CA2677796623
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945287_29945288del , CM000668.2:g.29945287_29945288del GRCh38
NC_000006.11:g.29913064_29913065del , CM000668.1:g.29913064_29913065del GRCh37
NC_000006.10:g.30021043_30021044del NCBI36
NG_029217.2:g.7823_7824del

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.976+6_976+7del ENSP00000492789.2:n.976+6_976+7del
ENST00000706892.1:n.2639_2640del
ENST00000706893.1:c.*77+6_*77+7del ENSP00000516609.1:n.*77+6_*77+7del
ENST00000706894.1:c.1099_1100del ENSP00000516610.1:p.Ser367LeufsTer?
ENST00000706895.1:n.1919_1920del
ENST00000706896.1:n.2389+6_2389+7del
ENST00000706897.1:n.1811+6_1811+7del
ENST00000706898.1:c.1111+6_1111+7del ENSP00000516611.1:n.1111+6_1111+7del
ENST00000706899.1:n.1947+6_1947+7del
ENST00000706900.1:c.1009+6_1009+7del ENSP00000516617.1:n.1009+6_1009+7del
ENST00000706901.1:c.1093+6_1093+7del ENSP00000516612.1:n.1093+6_1093+7del
ENST00000706902.1:c.1093+6_1093+7del ENSP00000516613.1:n.1093+6_1093+7del
ENST00000706903.1:c.1093+6_1093+7del ENSP00000516614.1:n.1093+6_1093+7del
ENST00000706904.1:c.1093+6_1093+7del ENSP00000516615.1:n.1093+6_1093+7del
ENST00000706905.1:c.1093+6_1093+7del ENSP00000516616.1:n.1093+6_1093+7del
ENST00000376809.10:c.1093+6_1093+7del MANE Select ENSP00000366005.5:n.1093+6_1093+7del
ENST00000376802.2:c.896-164_896-163del ENSP00000365998.2:n.896-164_896-163del
ENST00000376806.9:c.1111+6_1111+7del ENSP00000366002.5:n.1111+6_1111+7del
ENST00000376809.9:c.1093+6_1093+7del ENSP00000366005.5:n.1093+6_1093+7del
ENST00000396634.5:c.1093+6_1093+7del ENSP00000379873.1:n.1093+6_1093+7del
ENST00000495183.5:n.1332+6_1332+7del
ENST00000496081.5:n.1352+6_1352+7del
NM_002116.7:c.1093+6_1093+7del NP_002107.3:n.1093+6_1093+7del
NM_002116.8:c.1093+6_1093+7del MANE Select NP_002107.3:n.1093+6_1093+7del