Canonical Allele Identifier: CA1087349729
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v3: 6-29945306-G-T
gnomAD v4: 6-29945306-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945306G>T , CM000668.2:g.29945306G>T GRCh38
NC_000006.11:g.29913083G>T , CM000668.1:g.29913083G>T GRCh37
NC_000006.10:g.30021062G>T NCBI36
NG_029217.2:g.7842G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.976+25G>T ENSP00000492789.2:n.976+25G>T
ENST00000706892.1:n.2658G>T
ENST00000706893.1:c.*77+25G>T ENSP00000516609.1:n.*77+25G>T
ENST00000706894.1:c.1118G>T ENSP00000516610.1:p.Cys373Phe
ENST00000706895.1:n.1938G>T
ENST00000706896.1:n.2389+25G>T
ENST00000706897.1:n.1811+25G>T
ENST00000706898.1:c.1111+25G>T ENSP00000516611.1:n.1111+25G>T
ENST00000706899.1:n.1947+25G>T
ENST00000706900.1:c.1009+25G>T ENSP00000516617.1:n.1009+25G>T
ENST00000706901.1:c.1093+25G>T ENSP00000516612.1:n.1093+25G>T
ENST00000706902.1:c.1093+25G>T ENSP00000516613.1:n.1093+25G>T
ENST00000706903.1:c.1093+25G>T ENSP00000516614.1:n.1093+25G>T
ENST00000706904.1:c.1093+25G>T ENSP00000516615.1:n.1093+25G>T
ENST00000706905.1:c.1093+25G>T ENSP00000516616.1:n.1093+25G>T
ENST00000376809.10:c.1093+25G>T MANE Select ENSP00000366005.5:n.1093+25G>T
ENST00000376802.2:c.896-145G>T ENSP00000365998.2:n.896-145G>T
ENST00000376806.9:c.1111+25G>T ENSP00000366002.5:n.1111+25G>T
ENST00000376809.9:c.1093+25G>T ENSP00000366005.5:n.1093+25G>T
ENST00000396634.5:c.1093+25G>T ENSP00000379873.1:n.1093+25G>T
ENST00000495183.5:n.1332+25G>T
ENST00000496081.5:n.1352+25G>T
NM_002116.7:c.1093+25G>T NP_002107.3:n.1093+25G>T
NM_002116.8:c.1093+25G>T MANE Select NP_002107.3:n.1093+25G>T