Canonical Allele Identifier: CA363047936
Gene: HLA-A HGNC NCBI

Linked Data

gnomAD v4: 6-29944562-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944562G>T , CM000668.2:g.29944562G>T GRCh38
NC_000006.11:g.29912339G>T , CM000668.1:g.29912339G>T GRCh37
NC_000006.10:g.30020318G>T NCBI36
NG_029217.2:g.7098G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.895+165G>T ENSP00000492789.2:n.895+165G>T
ENST00000706892.1:n.1914G>T
ENST00000706893.1:c.992G>T ENSP00000516609.1:p.Ser331Ile
ENST00000706894.1:c.958G>T ENSP00000516610.1:p.Ala320Ser
ENST00000706895.1:n.1336G>T
ENST00000706896.1:n.1812G>T
ENST00000706897.1:n.1234G>T
ENST00000706898.1:c.958G>T ENSP00000516611.1:p.Ala320Ser
ENST00000706899.1:n.1812G>T
ENST00000706900.1:c.874G>T ENSP00000516617.1:p.Ala292Ser
ENST00000706901.1:c.958G>T ENSP00000516612.1:p.Ala320Ser
ENST00000706902.1:c.958G>T ENSP00000516613.1:p.Ala320Ser
ENST00000706903.1:c.958G>T ENSP00000516614.1:p.Ala320Ser
ENST00000706904.1:c.958G>T ENSP00000516615.1:p.Ala320Ser
ENST00000706905.1:c.958G>T ENSP00000516616.1:p.Ala320Ser
ENST00000376809.10:c.958G>T MANE Select ENSP00000366005.5:p.Ala320Ser
ENST00000638375.1:c.895+165G>T ENSP00000492789.1:n.895+165G>T
ENST00000376802.2:c.895+165G>T ENSP00000365998.2:n.895+165G>T
ENST00000376806.9:c.958G>T ENSP00000366002.5:p.Ala320Ser
ENST00000376809.9:c.958G>T ENSP00000366005.5:p.Ala320Ser
ENST00000396634.5:c.958G>T ENSP00000379873.1:p.Ala320Ser
ENST00000461903.1:n.1199G>T
ENST00000479320.5:n.1199G>T
ENST00000495183.5:n.1201G>T
ENST00000496081.5:n.775G>T
NM_002116.7:c.958G>T NP_002107.3:p.Ala320Ser
NM_002116.8:c.958G>T MANE Select NP_002107.3:p.Ala320Ser