Canonical Allele Identifier: CA2639833552
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516170del , CM000679.2:g.75516170del GRCh38
NC_000017.10:g.73512251del , CM000679.1:g.73512251del GRCh37
NC_000017.9:g.71023846del NCBI36
NG_013041.1:g.4643del
NG_033152.1:g.4416del

Transcript Alleles

HGVS Amino-acid Change
ENST00000434205.8:c.-299del ENSP00000406559.4:n.-299del
ENST00000679370.1:n.227del
ENST00000434205.7:c.-299del ENSP00000406559.3:n.-299del
XM_006721821.2:c.-464del XP_006721884.1:n.-464del