Canonical Allele Identifier: CA401029216
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521924T>G , CM000679.2:g.75521924T>G GRCh38
NC_000017.10:g.73518005T>G , CM000679.1:g.73518005T>G GRCh37
NC_000017.9:g.71029600T>G NCBI36
NG_013041.1:g.10397T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.843T>G MANE Select ENSP00000327487.6:p.Ser281Arg
ENST00000434205.8:c.540T>G ENSP00000406559.4:p.Ser180Arg
ENST00000545228.3:c.843T>G ENSP00000438169.3:p.Ser281Arg
ENST00000579449.2:n.642T>G
ENST00000580013.6:n.1046T>G
ENST00000679370.1:n.1424T>G
ENST00000679429.1:c.*301T>G ENSP00000505403.1:n.*301T>G
ENST00000679443.1:n.912T>G
ENST00000679782.1:c.843T>G ENSP00000505995.1:p.Ser281Arg
ENST00000679919.1:n.912T>G
ENST00000679928.1:c.*454T>G ENSP00000506071.1:n.*454T>G
ENST00000680528.1:n.868T>G
ENST00000680999.1:c.843T>G ENSP00000504984.1:p.Ser281Arg
ENST00000681282.1:c.*89T>G ENSP00000506339.1:n.*89T>G
ENST00000333213.10:c.843T>G ENSP00000327487.6:p.Ser281Arg
ENST00000578415.1:c.803T>G
ENST00000583173.5:c.459-83T>G ENSP00000463619.1:n.459-83T>G
NM_207346.2:c.843T>G NP_997229.2:p.Ser281Arg
XM_005257229.2:c.843T>G XP_005257286.1:p.Ser281Arg
XM_006721821.2:c.540T>G XP_006721884.1:p.Ser180Arg
XM_011524616.1:c.843T>G XP_011522918.1:p.Ser281Arg
XM_011524617.1:c.843T>G XP_011522919.1:p.Ser281Arg
XM_011524618.1:c.843T>G XP_011522920.1:p.Ser281Arg
XR_243646.2:n.873T>G
XM_005257229.4:c.843T>G XP_005257286.1:p.Ser281Arg
XR_243646.4:n.879T>G
NM_207346.3:c.843T>G MANE Select NP_997229.2:p.Ser281Arg