Canonical Allele Identifier: CA2677797295
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v4: 6-29945426-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945426T>A , CM000668.2:g.29945426T>A GRCh38
NC_000006.11:g.29913203T>A , CM000668.1:g.29913203T>A GRCh37
NC_000006.10:g.30021182T>A NCBI36
NG_029217.2:g.7962T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.977-25T>A ENSP00000492789.2:n.977-25T>A
ENST00000706892.1:n.2778T>A
ENST00000706893.1:c.*78-25T>A ENSP00000516609.1:n.*78-25T>A
ENST00000706894.1:c.*53T>A ENSP00000516610.1:n.*53T>A
ENST00000706895.1:n.2058T>A
ENST00000706896.1:n.2390-25T>A
ENST00000706897.1:n.1812-25T>A
ENST00000706898.1:c.1112-25T>A ENSP00000516611.1:n.1112-25T>A
ENST00000706899.1:n.1948-25T>A
ENST00000706900.1:c.1010-25T>A ENSP00000516617.1:n.1010-25T>A
ENST00000706901.1:c.1094-25T>A ENSP00000516612.1:n.1094-25T>A
ENST00000706902.1:c.1093+145T>A ENSP00000516613.1:n.1093+145T>A
ENST00000706903.1:c.1094-25T>A ENSP00000516614.1:n.1094-25T>A
ENST00000706904.1:c.1093+145T>A ENSP00000516615.1:n.1093+145T>A
ENST00000706905.1:c.1094-25T>A ENSP00000516616.1:n.1094-25T>A
ENST00000376809.10:c.1094-25T>A MANE Select ENSP00000366005.5:n.1094-25T>A
ENST00000376802.2:c.896-25T>A ENSP00000365998.2:n.896-25T>A
ENST00000376806.9:c.1112-25T>A ENSP00000366002.5:n.1112-25T>A
ENST00000376809.9:c.1094-25T>A ENSP00000366005.5:n.1094-25T>A
ENST00000396634.5:c.1094-25T>A ENSP00000379873.1:n.1094-25T>A
ENST00000495183.5:n.1333-25T>A
ENST00000496081.5:n.1353-25T>A
NM_002116.7:c.1094-25T>A NP_002107.3:n.1094-25T>A
NM_002116.8:c.1094-25T>A MANE Select NP_002107.3:n.1094-25T>A