Canonical Allele Identifier: CA2677951487
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271447del , CM000668.2:g.31271447del GRCh38
NC_000006.11:g.31239224del , CM000668.1:g.31239224del GRCh37
NC_000006.10:g.31347203del NCBI36
NG_029422.2:g.5687del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-97del MANE Select ENSP00000365402.5:n.344-97del
ENST00000376228.9:c.344-97del ENSP00000365402.5:n.344-97del
ENST00000376237.8:c.344-114del ENSP00000365412.4:n.344-114del
ENST00000383329.7:c.344-97del ENSP00000372819.3:n.344-97del
ENST00000415537.1:c.342-97del
ENST00000484378.1:n.516del
ENST00000487245.5:n.606del
ENST00000495835.1:n.533-97del
NM_002117.5:c.344-97del NP_002108.4:n.344-97del
NM_002117.6:c.344-97del MANE Select NP_002108.4:n.344-97del