Canonical Allele Identifier: CA2677950703
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270423_31270424del , CM000668.2:g.31270423_31270424del GRCh38
NC_000006.11:g.31238200_31238201del , CM000668.1:g.31238200_31238201del GRCh37
NC_000006.10:g.31346179_31346180del NCBI36
NG_029422.2:g.6708_6709del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.681_682del MANE Select ENSP00000365402.5:p.Cys227TrpfsTer?
ENST00000376228.9:c.681_682del ENSP00000365402.5:p.Cys227TrpfsTer?
ENST00000376237.8:c.*268_*269del ENSP00000365412.4:n.*268_*269del
ENST00000383329.7:c.681_682del ENSP00000372819.3:p.Cys227TrpfsTer?
ENST00000415537.1:c.664+15_664+16del
ENST00000487245.5:n.1040_1041del
ENST00000495835.1:n.870_871del
NM_002117.5:c.681_682del NP_002108.4:p.Cys227TrpfsTer?
NM_002117.6:c.681_682del MANE Select NP_002108.4:p.Cys227TrpfsTer?