Canonical Allele Identifier: CA2677950954
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270714_31270725del , CM000668.2:g.31270714_31270725del GRCh38
NC_000006.11:g.31238491_31238502del , CM000668.1:g.31238491_31238502del GRCh37
NC_000006.10:g.31346470_31346481del NCBI36
NG_029422.2:g.6407_6418del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-240_620-229del MANE Select ENSP00000365402.5:n.620-240_620-229del
ENST00000376228.9:c.620-240_620-229del ENSP00000365402.5:n.620-240_620-229del
ENST00000376237.8:c.*207-240_*207-229del ENSP00000365412.4:n.*207-240_*207-229del
ENST00000383329.7:c.620-240_620-229del ENSP00000372819.3:n.620-240_620-229del
ENST00000415537.1:c.618-240_618-229del
ENST00000487245.5:n.979-240_979-229del
ENST00000495835.1:n.809-240_809-229del
NM_002117.5:c.620-240_620-229del NP_002108.4:n.620-240_620-229del
NM_002117.6:c.620-240_620-229del MANE Select NP_002108.4:n.620-240_620-229del