Canonical Allele Identifier: CA401029194
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521919G>T , CM000679.2:g.75521919G>T GRCh38
NC_000017.10:g.73518000G>T , CM000679.1:g.73518000G>T GRCh37
NC_000017.9:g.71029595G>T NCBI36
NG_013041.1:g.10392G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.838G>T MANE Select ENSP00000327487.6:p.Glu280Ter
ENST00000434205.8:c.535G>T ENSP00000406559.4:p.Glu179Ter
ENST00000545228.3:c.838G>T ENSP00000438169.3:p.Glu280Ter
ENST00000579449.2:n.637G>T
ENST00000580013.6:n.1041G>T
ENST00000679370.1:n.1419G>T
ENST00000679429.1:c.*296G>T ENSP00000505403.1:n.*296G>T
ENST00000679443.1:n.907G>T
ENST00000679782.1:c.838G>T ENSP00000505995.1:p.Glu280Ter
ENST00000679919.1:n.907G>T
ENST00000679928.1:c.*449G>T ENSP00000506071.1:n.*449G>T
ENST00000680528.1:n.863G>T
ENST00000680999.1:c.838G>T ENSP00000504984.1:p.Glu280Ter
ENST00000681282.1:c.*84G>T ENSP00000506339.1:n.*84G>T
ENST00000333213.10:c.838G>T ENSP00000327487.6:p.Glu280Ter
ENST00000578415.1:c.798G>T
ENST00000583173.5:c.459-88G>T ENSP00000463619.1:n.459-88G>T
NM_207346.2:c.838G>T NP_997229.2:p.Glu280Ter
XM_005257229.2:c.838G>T XP_005257286.1:p.Glu280Ter
XM_006721821.2:c.535G>T XP_006721884.1:p.Glu179Ter
XM_011524616.1:c.838G>T XP_011522918.1:p.Glu280Ter
XM_011524617.1:c.838G>T XP_011522919.1:p.Glu280Ter
XM_011524618.1:c.838G>T XP_011522920.1:p.Glu280Ter
XR_243646.2:n.868G>T
XM_005257229.4:c.838G>T XP_005257286.1:p.Glu280Ter
XR_243646.4:n.874G>T
NM_207346.3:c.838G>T MANE Select NP_997229.2:p.Glu280Ter