Canonical Allele Identifier: CA2677950547
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270137_31270138del , CM000668.2:g.31270137_31270138del GRCh38
NC_000006.11:g.31237914_31237915del , CM000668.1:g.31237914_31237915del GRCh37
NC_000006.10:g.31345893_31345894del NCBI36
NG_029422.2:g.6994_6995del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.896-53_896-52del MANE Select ENSP00000365402.5:n.896-53_896-52del
ENST00000376228.9:c.896-53_896-52del ENSP00000365402.5:n.896-53_896-52del
ENST00000376237.8:c.*483-53_*483-52del ENSP00000365412.4:n.*483-53_*483-52del
ENST00000383329.7:c.896-53_896-52del ENSP00000372819.3:n.896-53_896-52del
ENST00000470363.5:n.214-53_214-52del
ENST00000487245.5:n.1255-53_1255-52del
NM_002117.5:c.896-53_896-52del NP_002108.4:n.896-53_896-52del
NM_002117.6:c.896-53_896-52del MANE Select NP_002108.4:n.896-53_896-52del