Canonical Allele Identifier: CA2770491518
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271128_31271129insTC , CM000668.2:g.31271128_31271129insTC GRCh38
NC_000006.11:g.31238905_31238906insTC , CM000668.1:g.31238905_31238906insTC GRCh37
NC_000006.10:g.31346884_31346885insTC NCBI36
NG_029422.2:g.6003_6004insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.563_564insGA MANE Select ENSP00000365402.5:p.Cys188TrpfsTer27
ENST00000376228.9:c.563_564insGA ENSP00000365402.5:p.Cys188TrpfsTer27
ENST00000376237.8:c.*150_*151insGA ENSP00000365412.4:n.*150_*151insGA
ENST00000383329.7:c.563_564insGA ENSP00000372819.3:p.Cys188TrpfsTer27
ENST00000415537.1:c.561_562insGA
ENST00000484378.1:n.832_833insGA
ENST00000487245.5:n.922_923insGA
ENST00000495835.1:n.752_753insGA
NM_002117.5:c.563_564insGA NP_002108.4:p.Cys188TrpfsTer27
NM_002117.6:c.563_564insGA MANE Select NP_002108.4:p.Cys188TrpfsTer27