Canonical Allele Identifier: CA2677949101
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268908del , CM000668.2:g.31268908del GRCh38
NC_000006.11:g.31236685del , CM000668.1:g.31236685del GRCh37
NC_000006.10:g.31344664del NCBI36
NG_029422.2:g.8224del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*261del MANE Select ENSP00000365402.5:n.*261del
ENST00000376228.9:c.*261del ENSP00000365402.5:n.*261del
ENST00000376237.8:c.*949del ENSP00000365412.4:n.*949del
ENST00000383329.7:c.*261del ENSP00000372819.3:n.*261del
ENST00000466892.5:n.595del
ENST00000470363.5:n.1120del
ENST00000487245.5:n.1721del
NM_002117.5:c.*261del NP_002108.4:n.*261del
NM_002117.6:c.*261del MANE Select NP_002108.4:n.*261del