Canonical Allele Identifier: CA2639833646
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516204_75516211del , CM000679.2:g.75516204_75516211del GRCh38
NC_000017.10:g.73512285_73512292del , CM000679.1:g.73512285_73512292del GRCh37
NC_000017.9:g.71023880_71023887del NCBI36
NG_013041.1:g.4677_4684del
NG_033152.1:g.4373_4380del

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-265_-258del ENSP00000406559.4:n.-265_-258del
ENST00000679370.1:n.261_268del
ENST00000434205.7:c.-265_-258del ENSP00000406559.3:n.-265_-258del
XM_006721821.2:c.-430_-423del XP_006721884.1:n.-430_-423del