Canonical Allele Identifier: CA2677950831
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270594_31270598del , CM000668.2:g.31270594_31270598del GRCh38
NC_000006.11:g.31238371_31238375del , CM000668.1:g.31238371_31238375del GRCh37
NC_000006.10:g.31346350_31346354del NCBI36
NG_029422.2:g.6534_6538del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-113_620-109del MANE Select ENSP00000365402.5:n.620-113_620-109del
ENST00000376228.9:c.620-113_620-109del ENSP00000365402.5:n.620-113_620-109del
ENST00000376237.8:c.*207-113_*207-109del ENSP00000365412.4:n.*207-113_*207-109del
ENST00000383329.7:c.620-113_620-109del ENSP00000372819.3:n.620-113_620-109del
ENST00000415537.1:c.618-113_618-109del
ENST00000487245.5:n.979-113_979-109del
ENST00000495835.1:n.809-113_809-109del
NM_002117.5:c.620-113_620-109del NP_002108.4:n.620-113_620-109del
NM_002117.6:c.620-113_620-109del MANE Select NP_002108.4:n.620-113_620-109del