Canonical Allele Identifier: CA2677951210
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271077_31271078insTA , CM000668.2:g.31271077_31271078insTA GRCh38
NC_000006.11:g.31238854_31238855insTA , CM000668.1:g.31238854_31238855insTA GRCh37
NC_000006.10:g.31346833_31346834insTA NCBI36
NG_029422.2:g.6054_6055insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.614_615insTA MANE Select ENSP00000365402.5:p.Ala206ThrfsTer9
ENST00000376228.9:c.614_615insTA ENSP00000365402.5:p.Ala206ThrfsTer9
ENST00000376237.8:c.*201_*202insTA ENSP00000365412.4:n.*201_*202insTA
ENST00000383329.7:c.614_615insTA ENSP00000372819.3:p.Ala206ThrfsTer9
ENST00000415537.1:c.612_613insTA
ENST00000487245.5:n.973_974insTA
ENST00000495835.1:n.803_804insTA
NM_002117.5:c.614_615insTA NP_002108.4:p.Ala206ThrfsTer9
NM_002117.6:c.614_615insTA MANE Select NP_002108.4:p.Ala206ThrfsTer9