Canonical Allele Identifier: CA2677950976
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270729_31270737del , CM000668.2:g.31270729_31270737del GRCh38
NC_000006.11:g.31238506_31238514del , CM000668.1:g.31238506_31238514del GRCh37
NC_000006.10:g.31346485_31346493del NCBI36
NG_029422.2:g.6395_6403del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-252_620-244del MANE Select ENSP00000365402.5:n.620-252_620-244del
ENST00000376228.9:c.620-252_620-244del ENSP00000365402.5:n.620-252_620-244del
ENST00000376237.8:c.*207-252_*207-244del ENSP00000365412.4:n.*207-252_*207-244del
ENST00000383329.7:c.620-252_620-244del ENSP00000372819.3:n.620-252_620-244del
ENST00000415537.1:c.618-252_618-244del
ENST00000487245.5:n.979-252_979-244del
ENST00000495835.1:n.809-252_809-244del
NM_002117.5:c.620-252_620-244del NP_002108.4:n.620-252_620-244del
NM_002117.6:c.620-252_620-244del MANE Select NP_002108.4:n.620-252_620-244del