Canonical Allele Identifier: CA2677951355
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271334_31271335insCCAA , CM000668.2:g.31271334_31271335insCCAA GRCh38
NC_000006.11:g.31239111_31239112insCCAA , CM000668.1:g.31239111_31239112insCCAA GRCh37
NC_000006.10:g.31347090_31347091insCCAA NCBI36
NG_029422.2:g.5797_5798insTTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.357_358insTTGG MANE Select ENSP00000365402.5:p.Gln120LeufsTer20
ENST00000376228.9:c.357_358insTTGG ENSP00000365402.5:p.Gln120LeufsTer20
ENST00000376237.8:c.344-4_344-3insTTGG ENSP00000365412.4:n.344-4_344-3insTTGG
ENST00000383329.7:c.357_358insTTGG ENSP00000372819.3:p.Gln120LeufsTer20
ENST00000415537.1:c.355_356insTTGG
ENST00000484378.1:n.626_627insTTGG
ENST00000487245.5:n.716_717insTTGG
ENST00000495835.1:n.546_547insTTGG
NM_002117.5:c.357_358insTTGG NP_002108.4:p.Gln120LeufsTer20
NM_002117.6:c.357_358insTTGG MANE Select NP_002108.4:p.Gln120LeufsTer20