Canonical Allele Identifier: CA2677951222
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271097dup , CM000668.2:g.31271097dup GRCh38
NC_000006.11:g.31238874dup , CM000668.1:g.31238874dup GRCh37
NC_000006.10:g.31346853dup NCBI36
NG_029422.2:g.6037dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.597dup MANE Select ENSP00000365402.5:p.Lys200GlufsTer21
ENST00000376228.9:c.597dup ENSP00000365402.5:p.Lys200GlufsTer21
ENST00000376237.8:c.*184dup ENSP00000365412.4:n.*184dup
ENST00000383329.7:c.597dup ENSP00000372819.3:p.Lys200GlufsTer21
ENST00000415537.1:c.595dup
ENST00000487245.5:n.956dup
ENST00000495835.1:n.786dup
NM_002117.5:c.597dup NP_002108.4:p.Lys200GlufsTer21
NM_002117.6:c.597dup MANE Select NP_002108.4:p.Lys200GlufsTer21