Canonical Allele Identifier: CA2639833618
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516192_75516193insG , CM000679.2:g.75516192_75516193insG GRCh38
NC_000017.10:g.73512273_73512274insG , CM000679.1:g.73512273_73512274insG GRCh37
NC_000017.9:g.71023868_71023869insG NCBI36
NG_013041.1:g.4665_4666insG
NG_033152.1:g.4391_4392insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-277_-276insG ENSP00000406559.4:n.-277_-276insG
ENST00000679370.1:n.249_250insG
ENST00000434205.7:c.-277_-276insG ENSP00000406559.3:n.-277_-276insG
XM_006721821.2:c.-442_-441insG XP_006721884.1:n.-442_-441insG