Canonical Allele Identifier: CA3693359
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs41549316
gnomAD v2: 6-29911186-T-C
gnomAD v3: 6-29943409-T-C
gnomAD v4: 6-29943409-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943409T>C , CM000668.2:g.29943409T>C GRCh38
NC_000006.11:g.29911186T>C , CM000668.1:g.29911186T>C GRCh37
NC_000006.10:g.30019165T>C NCBI36
NG_029217.2:g.5944T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.485T>C ENSP00000492789.2:p.Met162Thr
ENST00000706892.1:n.761T>C
ENST00000706893.1:c.485T>C ENSP00000516609.1:p.Met162Thr
ENST00000706894.1:c.485T>C ENSP00000516610.1:p.Met162Thr
ENST00000706895.1:n.761T>C
ENST00000706896.1:n.761T>C
ENST00000706897.1:n.761T>C
ENST00000706898.1:c.485T>C ENSP00000516611.1:p.Met162Thr
ENST00000706899.1:n.761T>C
ENST00000706900.1:c.401T>C ENSP00000516617.1:p.Met134Thr
ENST00000706901.1:c.485T>C ENSP00000516612.1:p.Met162Thr
ENST00000706902.1:c.485T>C ENSP00000516613.1:p.Met162Thr
ENST00000706903.1:c.485T>C ENSP00000516614.1:p.Met162Thr
ENST00000706904.1:c.485T>C ENSP00000516615.1:p.Met162Thr
ENST00000706905.1:c.485T>C ENSP00000516616.1:p.Met162Thr
ENST00000376809.10:c.485T>C MANE Select ENSP00000366005.5:p.Met162Thr
ENST00000638375.1:c.485T>C ENSP00000492789.1:p.Met162Thr
ENST00000376802.2:c.485T>C ENSP00000365998.2:p.Met162Thr
ENST00000376806.9:c.485T>C ENSP00000366002.5:p.Met162Thr
ENST00000376809.9:c.485T>C ENSP00000366005.5:p.Met162Thr
ENST00000396634.5:c.485T>C ENSP00000379873.1:p.Met162Thr
ENST00000461903.1:n.726T>C
ENST00000479320.5:n.726T>C
ENST00000495183.5:n.728T>C
ENST00000496081.5:n.302T>C
NM_002116.7:c.485T>C NP_002107.3:p.Met162Thr
NM_002116.8:c.485T>C MANE Select NP_002107.3:p.Met162Thr