Canonical Allele Identifier: CA2677951373
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271362dup , CM000668.2:g.31271362dup GRCh38
NC_000006.11:g.31239139dup , CM000668.1:g.31239139dup GRCh37
NC_000006.10:g.31347118dup NCBI36
NG_029422.2:g.5774dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-10dup MANE Select ENSP00000365402.5:n.344-10dup
ENST00000376228.9:c.344-10dup ENSP00000365402.5:n.344-10dup
ENST00000376237.8:c.344-27dup ENSP00000365412.4:n.344-27dup
ENST00000383329.7:c.344-10dup ENSP00000372819.3:n.344-10dup
ENST00000415537.1:c.342-10dup
ENST00000484378.1:n.603dup
ENST00000487245.5:n.693dup
ENST00000495835.1:n.533-10dup
NM_002117.5:c.344-10dup NP_002108.4:n.344-10dup
NM_002117.6:c.344-10dup MANE Select NP_002108.4:n.344-10dup