Canonical Allele Identifier: CA2275551188
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521724A= , CM000679.2:g.75521724A= GRCh38
NC_000017.10:g.73517805A= , CM000679.1:g.73517805A= GRCh37
NC_000017.9:g.71029400A= NCBI36
NG_013041.1:g.10197A=

Transcript Alleles

HGVS Amino-acid change
ENST00000333213.11:c.643A= MANE Select ENSP00000327487.6:p.Lys215=
ENST00000434205.8:c.340A= ENSP00000406559.4:p.Lys114=
ENST00000545228.3:c.643A= ENSP00000438169.3:p.Lys215=
ENST00000579449.2:n.442A=
ENST00000580013.6:n.846A=
ENST00000583818.2:c.697A= ENSP00000461928.2:n.697A=
ENST00000679370.1:n.1224A=
ENST00000679429.1:c.*101A= ENSP00000505403.1:n.*101A=
ENST00000679443.1:n.712A=
ENST00000679782.1:c.643A= ENSP00000505995.1:p.Lys215=
ENST00000679919.1:n.712A=
ENST00000679928.1:c.*254A= ENSP00000506071.1:n.*254A=
ENST00000680528.1:n.668A=
ENST00000680999.1:c.643A= ENSP00000504984.1:p.Lys215=
ENST00000681282.1:c.672A= ENSP00000506339.1:p.Pro224=
ENST00000333213.10:c.643A= ENSP00000327487.6:p.Lys215=
ENST00000578415.1:c.603A=
ENST00000583173.5:c.458+214A= ENSP00000463619.1:n.458+214A=
ENST00000583818.1:c.592A= ENSP00000461928.1:n.592A=
NM_207346.2:c.643A= NP_997229.2:p.Lys215=
XM_005257229.2:c.643A= XP_005257286.1:p.Lys215=
XM_006721821.2:c.340A= XP_006721884.1:p.Lys114=
XM_011524616.1:c.643A= XP_011522918.1:p.Lys215=
XM_011524617.1:c.643A= XP_011522919.1:p.Lys215=
XM_011524618.1:c.643A= XP_011522920.1:p.Lys215=
XR_243646.2:n.673A=
XM_005257229.4:c.643A= XP_005257286.1:p.Lys215=
XR_243646.4:n.679A=
NM_207346.3:c.643A= MANE Select NP_997229.2:p.Lys215=