Canonical Allele Identifier: CA401028157
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521411C>G , CM000679.2:g.75521411C>G GRCh38
NC_000017.10:g.73517492C>G , CM000679.1:g.73517492C>G GRCh37
NC_000017.9:g.71029087C>G NCBI36
NG_013041.1:g.9884C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.524C>G MANE Select ENSP00000327487.6:p.Ser175Cys
ENST00000434205.8:c.221C>G ENSP00000406559.4:p.Ser74Cys
ENST00000545228.3:c.524C>G ENSP00000438169.3:p.Ser175Cys
ENST00000579449.2:n.323C>G
ENST00000580013.6:n.533C>G
ENST00000583818.2:c.578C>G ENSP00000461928.2:n.578C>G
ENST00000679370.1:n.911C>G
ENST00000679429.1:c.516C>G ENSP00000505403.1:p.Leu172=
ENST00000679443.1:n.399C>G
ENST00000679782.1:c.524C>G ENSP00000505995.1:p.Ser175Cys
ENST00000679919.1:n.399C>G
ENST00000679928.1:c.*135C>G ENSP00000506071.1:n.*135C>G
ENST00000680528.1:n.549C>G
ENST00000680999.1:c.524C>G ENSP00000504984.1:p.Ser175Cys
ENST00000681282.1:c.524C>G ENSP00000506339.1:p.Ser175Cys
ENST00000333213.10:c.524C>G ENSP00000327487.6:p.Ser175Cys
ENST00000578415.1:c.484C>G
ENST00000580013.5:n.541C>G
ENST00000583173.5:c.359C>G ENSP00000463619.1:p.Ser120Cys
ENST00000583818.1:c.473C>G ENSP00000461928.1:n.473C>G
NM_207346.2:c.524C>G NP_997229.2:p.Ser175Cys
XM_005257229.2:c.524C>G XP_005257286.1:p.Ser175Cys
XM_006721821.2:c.221C>G XP_006721884.1:p.Ser74Cys
XM_011524616.1:c.524C>G XP_011522918.1:p.Ser175Cys
XM_011524617.1:c.524C>G XP_011522919.1:p.Ser175Cys
XM_011524618.1:c.524C>G XP_011522920.1:p.Ser175Cys
XR_243646.2:n.554C>G
XM_005257229.4:c.524C>G XP_005257286.1:p.Ser175Cys
XR_243646.4:n.560C>G
NM_207346.3:c.524C>G MANE Select NP_997229.2:p.Ser175Cys