Canonical Allele Identifier: CA401028778
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521801C>A , CM000679.2:g.75521801C>A GRCh38
NC_000017.10:g.73517882C>A , CM000679.1:g.73517882C>A GRCh37
NC_000017.9:g.71029477C>A NCBI36
NG_013041.1:g.10274C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.720C>A MANE Select ENSP00000327487.6:p.Cys240Ter
ENST00000434205.8:c.417C>A ENSP00000406559.4:p.Cys139Ter
ENST00000545228.3:c.720C>A ENSP00000438169.3:p.Cys240Ter
ENST00000579449.2:n.519C>A
ENST00000580013.6:n.923C>A
ENST00000583818.2:c.774C>A ENSP00000461928.2:n.774C>A
ENST00000679370.1:n.1301C>A
ENST00000679429.1:c.*178C>A ENSP00000505403.1:n.*178C>A
ENST00000679443.1:n.789C>A
ENST00000679782.1:c.720C>A ENSP00000505995.1:p.Cys240Ter
ENST00000679919.1:n.789C>A
ENST00000679928.1:c.*331C>A ENSP00000506071.1:n.*331C>A
ENST00000680528.1:n.745C>A
ENST00000680999.1:c.720C>A ENSP00000504984.1:p.Cys240Ter
ENST00000681282.1:c.749C>A ENSP00000506339.1:p.Ala250Asp
ENST00000333213.10:c.720C>A ENSP00000327487.6:p.Cys240Ter
ENST00000578415.1:c.680C>A
ENST00000583173.5:c.459-206C>A ENSP00000463619.1:n.459-206C>A
ENST00000583818.1:c.669C>A ENSP00000461928.1:n.669C>A
NM_207346.2:c.720C>A NP_997229.2:p.Cys240Ter
XM_005257229.2:c.720C>A XP_005257286.1:p.Cys240Ter
XM_006721821.2:c.417C>A XP_006721884.1:p.Cys139Ter
XM_011524616.1:c.720C>A XP_011522918.1:p.Cys240Ter
XM_011524617.1:c.720C>A XP_011522919.1:p.Cys240Ter
XM_011524618.1:c.720C>A XP_011522920.1:p.Cys240Ter
XR_243646.2:n.750C>A
XM_005257229.4:c.720C>A XP_005257286.1:p.Cys240Ter
XR_243646.4:n.756C>A
NM_207346.3:c.720C>A MANE Select NP_997229.2:p.Cys240Ter