Canonical Allele Identifier: CA2677951498
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271457_31271458del , CM000668.2:g.31271457_31271458del GRCh38
NC_000006.11:g.31239234_31239235del , CM000668.1:g.31239234_31239235del GRCh37
NC_000006.10:g.31347213_31347214del NCBI36
NG_029422.2:g.5676_5677del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-108_344-107del MANE Select ENSP00000365402.5:n.344-108_344-107del
ENST00000376228.9:c.344-108_344-107del ENSP00000365402.5:n.344-108_344-107del
ENST00000376237.8:c.344-125_344-124del ENSP00000365412.4:n.344-125_344-124del
ENST00000383329.7:c.344-108_344-107del ENSP00000372819.3:n.344-108_344-107del
ENST00000415537.1:c.342-108_342-107del
ENST00000484378.1:n.505_506del
ENST00000487245.5:n.595_596del
ENST00000495835.1:n.533-108_533-107del
NM_002117.5:c.344-108_344-107del NP_002108.4:n.344-108_344-107del
NM_002117.6:c.344-108_344-107del MANE Select NP_002108.4:n.344-108_344-107del