Canonical Allele Identifier: CA136025112
Gene: HLA-A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs199474644

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NM_002116.7:c.896-47del VV NP_002107.3:p.=
NM_002116.8:c.896-47del VV MANE Preferred
ENST00000376802.2:c.895+56del ENSP00000365998.2:p.=
ENST00000376806.9:c.896-47del ENSP00000366002.5:p.=
ENST00000376809.9:c.896-47del ENSP00000366005.5:p.=
ENST00000396634.5:c.896-47del ENSP00000379873.1:p.=
ENST00000461903.1:n.1137-47del
ENST00000479320.5:n.1137-47del
ENST00000495183.5:n.1139-47del
ENST00000496081.5:n.713-47del