Canonical Allele Identifier: CA2275551295
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521915C= , CM000679.2:g.75521915C= GRCh38
NC_000017.10:g.73517996C= , CM000679.1:g.73517996C= GRCh37
NC_000017.9:g.71029591C= NCBI36
NG_013041.1:g.10388C=

Transcript Alleles

HGVS Amino-acid change
ENST00000333213.11:c.834C= MANE Select ENSP00000327487.6:p.Ser278=
ENST00000434205.8:c.531C= ENSP00000406559.4:p.Ser177=
ENST00000545228.3:c.834C= ENSP00000438169.3:p.Ser278=
ENST00000579449.2:n.633C=
ENST00000580013.6:n.1037C=
ENST00000679370.1:n.1415C=
ENST00000679429.1:c.*292C= ENSP00000505403.1:n.*292C=
ENST00000679443.1:n.903C=
ENST00000679782.1:c.834C= ENSP00000505995.1:p.Ser278=
ENST00000679919.1:n.903C=
ENST00000679928.1:c.*445C= ENSP00000506071.1:n.*445C=
ENST00000680528.1:n.859C=
ENST00000680999.1:c.834C= ENSP00000504984.1:p.Ser278=
ENST00000681282.1:c.*80C= ENSP00000506339.1:n.*80C=
ENST00000333213.10:c.834C= ENSP00000327487.6:p.Ser278=
ENST00000578415.1:c.794C=
ENST00000583173.5:c.459-92C= ENSP00000463619.1:n.459-92C=
NM_207346.2:c.834C= NP_997229.2:p.Ser278=
XM_005257229.2:c.834C= XP_005257286.1:p.Ser278=
XM_006721821.2:c.531C= XP_006721884.1:p.Ser177=
XM_011524616.1:c.834C= XP_011522918.1:p.Ser278=
XM_011524617.1:c.834C= XP_011522919.1:p.Ser278=
XM_011524618.1:c.834C= XP_011522920.1:p.Ser278=
XR_243646.2:n.864C=
XM_005257229.4:c.834C= XP_005257286.1:p.Ser278=
XR_243646.4:n.870C=
NM_207346.3:c.834C= MANE Select NP_997229.2:p.Ser278=