Canonical Allele Identifier: CA2639833947
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516273_75516275del , CM000679.2:g.75516273_75516275del GRCh38
NC_000017.10:g.73512354_73512356del , CM000679.1:g.73512354_73512356del GRCh37
NC_000017.9:g.71023949_71023951del NCBI36
NG_013041.1:g.4746_4748del
NG_033152.1:g.4310_4312del

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-196_-194del ENSP00000406559.4:n.-196_-194del
ENST00000679370.1:n.330_332del
ENST00000434205.7:c.-196_-194del ENSP00000406559.3:n.-196_-194del
XM_006721821.2:c.-361_-359del XP_006721884.1:n.-361_-359del