Canonical Allele Identifier: CA2677951251
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271133_31271134insTC , CM000668.2:g.31271133_31271134insTC GRCh38
NC_000006.11:g.31238910_31238911insTC , CM000668.1:g.31238910_31238911insTC GRCh37
NC_000006.10:g.31346889_31346890insTC NCBI36
NG_029422.2:g.5998_5999insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.558_559insGA MANE Select ENSP00000365402.5:p.Thr187GlufsTer28
ENST00000376228.9:c.558_559insGA ENSP00000365402.5:p.Thr187GlufsTer28
ENST00000376237.8:c.*145_*146insGA ENSP00000365412.4:n.*145_*146insGA
ENST00000383329.7:c.558_559insGA ENSP00000372819.3:p.Thr187GlufsTer28
ENST00000415537.1:c.556_557insGA
ENST00000484378.1:n.827_828insGA
ENST00000487245.5:n.917_918insGA
ENST00000495835.1:n.747_748insGA
NM_002117.5:c.558_559insGA NP_002108.4:p.Thr187GlufsTer28
NM_002117.6:c.558_559insGA MANE Select NP_002108.4:p.Thr187GlufsTer28