Canonical Allele Identifier: CA2677796761
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945313_29945314insCTG , CM000668.2:g.29945313_29945314insCTG GRCh38
NC_000006.11:g.29913090_29913091insCTG , CM000668.1:g.29913090_29913091insCTG GRCh37
NC_000006.10:g.30021069_30021070insCTG NCBI36
NG_029217.2:g.7849_7850insCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.976+32_976+33insCTG ENSP00000492789.2:n.976+32_976+33insCTG
ENST00000706892.1:n.2665_2666insCTG
ENST00000706893.1:c.*77+32_*77+33insCTG ENSP00000516609.1:n.*77+32_*77+33insCTG
ENST00000706894.1:c.1125_1126insCTG ENSP00000516610.1:p.Gly375_Cys376insLeu
ENST00000706895.1:n.1945_1946insCTG
ENST00000706896.1:n.2389+32_2389+33insCTG
ENST00000706897.1:n.1811+32_1811+33insCTG
ENST00000706898.1:c.1111+32_1111+33insCTG ENSP00000516611.1:n.1111+32_1111+33insCTG
ENST00000706899.1:n.1947+32_1947+33insCTG
ENST00000706900.1:c.1009+32_1009+33insCTG ENSP00000516617.1:n.1009+32_1009+33insCTG
ENST00000706901.1:c.1093+32_1093+33insCTG ENSP00000516612.1:n.1093+32_1093+33insCTG
ENST00000706902.1:c.1093+32_1093+33insCTG ENSP00000516613.1:n.1093+32_1093+33insCTG
ENST00000706903.1:c.1093+32_1093+33insCTG ENSP00000516614.1:n.1093+32_1093+33insCTG
ENST00000706904.1:c.1093+32_1093+33insCTG ENSP00000516615.1:n.1093+32_1093+33insCTG
ENST00000706905.1:c.1093+32_1093+33insCTG ENSP00000516616.1:n.1093+32_1093+33insCTG
ENST00000376809.10:c.1093+32_1093+33insCTG MANE Select ENSP00000366005.5:n.1093+32_1093+33insCTG
ENST00000376802.2:c.896-138_896-137insCTG ENSP00000365998.2:n.896-138_896-137insCTG
ENST00000376806.9:c.1111+32_1111+33insCTG ENSP00000366002.5:n.1111+32_1111+33insCTG
ENST00000376809.9:c.1093+32_1093+33insCTG ENSP00000366005.5:n.1093+32_1093+33insCTG
ENST00000396634.5:c.1093+32_1093+33insCTG ENSP00000379873.1:n.1093+32_1093+33insCTG
ENST00000495183.5:n.1332+32_1332+33insCTG
ENST00000496081.5:n.1352+32_1352+33insCTG
NM_002116.7:c.1093+32_1093+33insCTG NP_002107.3:n.1093+32_1093+33insCTG
NM_002116.8:c.1093+32_1093+33insCTG MANE Select NP_002107.3:n.1093+32_1093+33insCTG