Canonical Allele Identifier: CA2677950452
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270108_31270111del , CM000668.2:g.31270108_31270111del GRCh38
NC_000006.11:g.31237885_31237888del , CM000668.1:g.31237885_31237888del GRCh37
NC_000006.10:g.31345864_31345867del NCBI36
NG_029422.2:g.7021_7024del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.896-26_896-23del MANE Select ENSP00000365402.5:n.896-26_896-23del
ENST00000376228.9:c.896-26_896-23del ENSP00000365402.5:n.896-26_896-23del
ENST00000376237.8:c.*483-26_*483-23del ENSP00000365412.4:n.*483-26_*483-23del
ENST00000383329.7:c.896-26_896-23del ENSP00000372819.3:n.896-26_896-23del
ENST00000470363.5:n.214-26_214-23del
ENST00000487245.5:n.1255-26_1255-23del
NM_002117.5:c.896-26_896-23del NP_002108.4:n.896-26_896-23del
NM_002117.6:c.896-26_896-23del MANE Select NP_002108.4:n.896-26_896-23del