Canonical Allele Identifier: CA2770491514
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271111_31271112insAGC , CM000668.2:g.31271111_31271112insAGC GRCh38
NC_000006.11:g.31238888_31238889insAGC , CM000668.1:g.31238888_31238889insAGC GRCh37
NC_000006.10:g.31346867_31346868insAGC NCBI36
NG_029422.2:g.6021_6022insCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.581_582insCTG MANE Select ENSP00000365402.5:p.Arg194SerfsTer2
ENST00000376228.9:c.581_582insCTG ENSP00000365402.5:p.Arg194SerfsTer2
ENST00000376237.8:c.*168_*169insCTG ENSP00000365412.4:n.*168_*169insCTG
ENST00000383329.7:c.581_582insCTG ENSP00000372819.3:p.Arg194SerfsTer2
ENST00000415537.1:c.579_580insCTG
ENST00000484378.1:n.850_851insCTG
ENST00000487245.5:n.940_941insCTG
ENST00000495835.1:n.770_771insCTG
NM_002117.5:c.581_582insCTG NP_002108.4:p.Arg194SerfsTer2
NM_002117.6:c.581_582insCTG MANE Select NP_002108.4:p.Arg194SerfsTer2