Canonical Allele Identifier: CA2677951347
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271324_31271325insT , CM000668.2:g.31271324_31271325insT GRCh38
NC_000006.11:g.31239101_31239102insT , CM000668.1:g.31239101_31239102insT GRCh37
NC_000006.10:g.31347080_31347081insT NCBI36
NG_029422.2:g.5807_5808insA

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.367_368insA MANE Select ENSP00000365402.5:p.Ser123TyrfsTer16
ENST00000376228.9:c.367_368insA ENSP00000365402.5:p.Ser123TyrfsTer16
ENST00000376237.8:c.350_351insA ENSP00000365412.4:p.Trp118LeufsTer28
ENST00000383329.7:c.367_368insA ENSP00000372819.3:p.Ser123TyrfsTer16
ENST00000415537.1:c.365_366insA
ENST00000484378.1:n.636_637insA
ENST00000487245.5:n.726_727insA
ENST00000495835.1:n.556_557insA
NM_002117.5:c.367_368insA NP_002108.4:p.Ser123TyrfsTer16
NM_002117.6:c.367_368insA MANE Select NP_002108.4:p.Ser123TyrfsTer16