Canonical Allele Identifier: CA2677950836
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270598_31270603del , CM000668.2:g.31270598_31270603del GRCh38
NC_000006.11:g.31238375_31238380del , CM000668.1:g.31238375_31238380del GRCh37
NC_000006.10:g.31346354_31346359del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-118_620-113del MANE Select ENSP00000365402.5:n.620-118_620-113del
ENST00000376228.9:c.620-118_620-113del ENSP00000365402.5:n.620-118_620-113del
ENST00000376237.8:c.*207-118_*207-113del ENSP00000365412.4:n.*207-118_*207-113del
ENST00000383329.7:c.620-118_620-113del ENSP00000372819.3:n.620-118_620-113del
ENST00000415537.1:c.618-118_618-113del
ENST00000487245.5:n.979-118_979-113del
ENST00000495835.1:n.809-118_809-113del
NM_002117.5:c.620-118_620-113del NP_002108.4:n.620-118_620-113del
NM_002117.6:c.620-118_620-113del MANE Select NP_002108.4:n.620-118_620-113del