Canonical Allele Identifier: CA1087343953
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943956_29943990del , CM000668.2:g.29943956_29943990del GRCh38
NC_000006.11:g.29911733_29911767del , CM000668.1:g.29911733_29911767del GRCh37
NC_000006.10:g.30019712_30019746del NCBI36
NG_029217.2:g.6492_6526del

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.620-166_620-132del ENSP00000492789.2:n.620-166_620-132del
ENST00000706892.1:n.1308_1342del
ENST00000706893.1:c.620-166_620-132del ENSP00000516609.1:n.620-166_620-132del
ENST00000706894.1:c.620-166_620-132del ENSP00000516610.1:n.620-166_620-132del
ENST00000706895.1:n.896-166_896-132del
ENST00000706896.1:n.1308_1342del
ENST00000706897.1:n.896-166_896-132del
ENST00000706898.1:c.620-166_620-132del ENSP00000516611.1:n.620-166_620-132del
ENST00000706899.1:n.1308_1342del
ENST00000706900.1:c.536-166_536-132del ENSP00000516617.1:n.536-166_536-132del
ENST00000706901.1:c.620-166_620-132del ENSP00000516612.1:n.620-166_620-132del
ENST00000706902.1:c.620-166_620-132del ENSP00000516613.1:n.620-166_620-132del
ENST00000706903.1:c.620-166_620-132del ENSP00000516614.1:n.620-166_620-132del
ENST00000706904.1:c.620-166_620-132del ENSP00000516615.1:n.620-166_620-132del
ENST00000706905.1:c.620-166_620-132del ENSP00000516616.1:n.620-166_620-132del
ENST00000376809.10:c.620-166_620-132del MANE Select ENSP00000366005.5:n.620-166_620-132del
ENST00000638375.1:c.620-166_620-132del ENSP00000492789.1:n.620-166_620-132del
ENST00000376802.2:c.620-166_620-132del ENSP00000365998.2:n.620-166_620-132del
ENST00000376806.9:c.620-166_620-132del ENSP00000366002.5:n.620-166_620-132del
ENST00000376809.9:c.620-166_620-132del ENSP00000366005.5:n.620-166_620-132del
ENST00000396634.5:c.620-166_620-132del ENSP00000379873.1:n.620-166_620-132del
ENST00000461903.1:n.861-166_861-132del
ENST00000479320.5:n.861-166_861-132del
ENST00000495183.5:n.863-166_863-132del
ENST00000496081.5:n.437-166_437-132del
NM_002116.7:c.620-166_620-132del NP_002107.3:n.620-166_620-132del
NM_002116.8:c.620-166_620-132del MANE Select NP_002107.3:n.620-166_620-132del