Canonical Allele Identifier: CA2639833760
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516239_75516335del , CM000679.2:g.75516239_75516335del GRCh38
NC_000017.10:g.73512320_73512416del , CM000679.1:g.73512320_73512416del GRCh37
NC_000017.9:g.71023915_71024011del NCBI36
NG_013041.1:g.4712_4808del
NG_033152.1:g.4257_4353del

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-230_-134del ENSP00000406559.4:n.-230_-134del
ENST00000679370.1:n.296_392del
ENST00000434205.7:c.-230_-134del ENSP00000406559.3:n.-230_-134del
XM_006721821.2:c.-395_-299del XP_006721884.1:n.-395_-299del