Canonical Allele Identifier: CA1087452513
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269989_31269990insG , CM000668.2:g.31269989_31269990insG GRCh38
NC_000006.11:g.31237766_31237767insG , CM000668.1:g.31237766_31237767insG GRCh37
NC_000006.10:g.31345745_31345746insG NCBI36
NG_029422.2:g.7142_7143insC

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.991_992insC MANE Select ENSP00000365402.5:p.Met331ThrfsTer4
ENST00000376228.9:c.991_992insC ENSP00000365402.5:p.Met331ThrfsTer4
ENST00000376237.8:c.*578_*579insC ENSP00000365412.4:n.*578_*579insC
ENST00000383329.7:c.991_992insC ENSP00000372819.3:p.Met331ThrfsTer4
ENST00000470363.5:n.309_310insC
ENST00000487245.5:n.1350_1351insC
NM_002117.5:c.991_992insC NP_002108.4:p.Met331ThrfsTer4
NM_002117.6:c.991_992insC MANE Select NP_002108.4:p.Met331ThrfsTer4