Canonical Allele Identifier: CA1087344212
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944005_29944020del , CM000668.2:g.29944005_29944020del GRCh38
NC_000006.11:g.29911782_29911797del , CM000668.1:g.29911782_29911797del GRCh37
NC_000006.10:g.30019761_30019776del NCBI36
NG_029217.2:g.6541_6556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.620-117_620-102del ENSP00000492789.2:n.620-117_620-102del
ENST00000706892.1:n.1357_1372del
ENST00000706893.1:c.620-117_620-102del ENSP00000516609.1:n.620-117_620-102del
ENST00000706894.1:c.620-117_620-102del ENSP00000516610.1:n.620-117_620-102del
ENST00000706895.1:n.896-117_896-102del
ENST00000706896.1:n.1357_1372del
ENST00000706897.1:n.896-117_896-102del
ENST00000706898.1:c.620-117_620-102del ENSP00000516611.1:n.620-117_620-102del
ENST00000706899.1:n.1357_1372del
ENST00000706900.1:c.536-117_536-102del ENSP00000516617.1:n.536-117_536-102del
ENST00000706901.1:c.620-117_620-102del ENSP00000516612.1:n.620-117_620-102del
ENST00000706902.1:c.620-117_620-102del ENSP00000516613.1:n.620-117_620-102del
ENST00000706903.1:c.620-117_620-102del ENSP00000516614.1:n.620-117_620-102del
ENST00000706904.1:c.620-117_620-102del ENSP00000516615.1:n.620-117_620-102del
ENST00000706905.1:c.620-117_620-102del ENSP00000516616.1:n.620-117_620-102del
ENST00000376809.10:c.620-117_620-102del MANE Select ENSP00000366005.5:n.620-117_620-102del
ENST00000638375.1:c.620-117_620-102del ENSP00000492789.1:n.620-117_620-102del
ENST00000376802.2:c.620-117_620-102del ENSP00000365998.2:n.620-117_620-102del
ENST00000376806.9:c.620-117_620-102del ENSP00000366002.5:n.620-117_620-102del
ENST00000376809.9:c.620-117_620-102del ENSP00000366005.5:n.620-117_620-102del
ENST00000396634.5:c.620-117_620-102del ENSP00000379873.1:n.620-117_620-102del
ENST00000461903.1:n.861-117_861-102del
ENST00000479320.5:n.861-117_861-102del
ENST00000495183.5:n.863-117_863-102del
ENST00000496081.5:n.437-117_437-102del
NM_002116.7:c.620-117_620-102del NP_002107.3:n.620-117_620-102del
NM_002116.8:c.620-117_620-102del MANE Select NP_002107.3:n.620-117_620-102del