Canonical Allele Identifier: CA2677951348
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271327_31271328insGTACA , CM000668.2:g.31271327_31271328insGTACA GRCh38
NC_000006.11:g.31239104_31239105insGTACA , CM000668.1:g.31239104_31239105insGTACA GRCh37
NC_000006.10:g.31347083_31347084insGTACA NCBI36
NG_029422.2:g.5807_5808insACTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.367_368insACTGT MANE Select ENSP00000365402.5:p.Ser123TyrfsTer30
ENST00000376228.9:c.367_368insACTGT ENSP00000365402.5:p.Ser123TyrfsTer30
ENST00000376237.8:c.350_351insACTGT ENSP00000365412.4:p.Trp118LeufsTer?
ENST00000383329.7:c.367_368insACTGT ENSP00000372819.3:p.Ser123TyrfsTer30
ENST00000415537.1:c.365_366insACTGT
ENST00000484378.1:n.636_637insACTGT
ENST00000487245.5:n.726_727insACTGT
ENST00000495835.1:n.556_557insACTGT
NM_002117.5:c.367_368insACTGT NP_002108.4:p.Ser123TyrfsTer30
NM_002117.6:c.367_368insACTGT MANE Select NP_002108.4:p.Ser123TyrfsTer30