Canonical Allele Identifier: CA2639833529
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516145_75516148del , CM000679.2:g.75516145_75516148del GRCh38
NC_000017.10:g.73512226_73512229del , CM000679.1:g.73512226_73512229del GRCh37
NC_000017.9:g.71023821_71023824del NCBI36
NG_013041.1:g.4618_4621del
NG_033152.1:g.4436_4439del

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-324_-321del ENSP00000406559.4:n.-324_-321del
ENST00000679370.1:n.202_205del
ENST00000434205.7:c.-324_-321del ENSP00000406559.3:n.-324_-321del
XM_006721821.2:c.-489_-486del XP_006721884.1:n.-489_-486del