Canonical Allele Identifier: CA823768868
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs1198461078

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944453_29944455del , CM000668.2:g.29944453_29944455del GRCh38
NC_000006.11:g.29912230_29912232del , CM000668.1:g.29912230_29912232del GRCh37
NC_000006.10:g.30020209_30020211del NCBI36
NG_029217.2:g.6989_6991del

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.895+56_895+58del ENSP00000492789.2:n.895+56_895+58del
ENST00000706892.1:n.1805_1807del
ENST00000706893.1:c.896-13_896-11del ENSP00000516609.1:n.896-13_896-11del
ENST00000706894.1:c.896-47_896-45del ENSP00000516610.1:n.896-47_896-45del
ENST00000706895.1:n.1227_1229del
ENST00000706896.1:n.1750-47_1750-45del
ENST00000706897.1:n.1172-47_1172-45del
ENST00000706898.1:c.896-47_896-45del ENSP00000516611.1:n.896-47_896-45del
ENST00000706899.1:n.1750-47_1750-45del
ENST00000706900.1:c.812-47_812-45del ENSP00000516617.1:n.812-47_812-45del
ENST00000706901.1:c.896-47_896-45del ENSP00000516612.1:n.896-47_896-45del
ENST00000706902.1:c.896-47_896-45del ENSP00000516613.1:n.896-47_896-45del
ENST00000706903.1:c.896-47_896-45del ENSP00000516614.1:n.896-47_896-45del
ENST00000706904.1:c.896-47_896-45del ENSP00000516615.1:n.896-47_896-45del
ENST00000706905.1:c.896-47_896-45del ENSP00000516616.1:n.896-47_896-45del
ENST00000376809.10:c.896-47_896-45del MANE Select ENSP00000366005.5:n.896-47_896-45del
ENST00000638375.1:c.895+56_895+58del ENSP00000492789.1:n.895+56_895+58del
ENST00000376802.2:c.895+56_895+58del ENSP00000365998.2:n.895+56_895+58del
ENST00000376806.9:c.896-47_896-45del ENSP00000366002.5:n.896-47_896-45del
ENST00000376809.9:c.896-47_896-45del ENSP00000366005.5:n.896-47_896-45del
ENST00000396634.5:c.896-47_896-45del ENSP00000379873.1:n.896-47_896-45del
ENST00000461903.1:n.1137-47_1137-45del
ENST00000479320.5:n.1137-47_1137-45del
ENST00000495183.5:n.1139-47_1139-45del
ENST00000496081.5:n.713-47_713-45del
NM_002116.7:c.896-47_896-45del NP_002107.3:n.896-47_896-45del
NM_002116.8:c.896-47_896-45del MANE Select NP_002107.3:n.896-47_896-45del