Canonical Allele Identifier: CA401028352
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521498G>C , CM000679.2:g.75521498G>C GRCh38
NC_000017.10:g.73517579G>C , CM000679.1:g.73517579G>C GRCh37
NC_000017.9:g.71029174G>C NCBI36
NG_013041.1:g.9971G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.611G>C MANE Select ENSP00000327487.6:p.Ser204Thr
ENST00000434205.8:c.308G>C ENSP00000406559.4:p.Ser103Thr
ENST00000545228.3:c.611G>C ENSP00000438169.3:p.Ser204Thr
ENST00000579449.2:n.410G>C
ENST00000580013.6:n.620G>C
ENST00000583818.2:c.665G>C ENSP00000461928.2:n.665G>C
ENST00000679370.1:n.998G>C
ENST00000679429.1:c.*69G>C ENSP00000505403.1:n.*69G>C
ENST00000679443.1:n.486G>C
ENST00000679782.1:c.611G>C ENSP00000505995.1:p.Ser204Thr
ENST00000679919.1:n.486G>C
ENST00000679928.1:c.*222G>C ENSP00000506071.1:n.*222G>C
ENST00000680528.1:n.636G>C
ENST00000680999.1:c.611G>C ENSP00000504984.1:p.Ser204Thr
ENST00000681282.1:c.611G>C ENSP00000506339.1:p.Ser204Thr
ENST00000333213.10:c.611G>C ENSP00000327487.6:p.Ser204Thr
ENST00000578415.1:c.571G>C
ENST00000583173.5:c.446G>C ENSP00000463619.1:p.Ser149Thr
ENST00000583818.1:c.560G>C ENSP00000461928.1:n.560G>C
NM_207346.2:c.611G>C NP_997229.2:p.Ser204Thr
XM_005257229.2:c.611G>C XP_005257286.1:p.Ser204Thr
XM_006721821.2:c.308G>C XP_006721884.1:p.Ser103Thr
XM_011524616.1:c.611G>C XP_011522918.1:p.Ser204Thr
XM_011524617.1:c.611G>C XP_011522919.1:p.Ser204Thr
XM_011524618.1:c.611G>C XP_011522920.1:p.Ser204Thr
XR_243646.2:n.641G>C
XM_005257229.4:c.611G>C XP_005257286.1:p.Ser204Thr
XR_243646.4:n.647G>C
NM_207346.3:c.611G>C MANE Select NP_997229.2:p.Ser204Thr