Canonical Allele Identifier: CA2275551189
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521725A= , CM000679.2:g.75521725A= GRCh38
NC_000017.10:g.73517806A= , CM000679.1:g.73517806A= GRCh37
NC_000017.9:g.71029401A= NCBI36
NG_013041.1:g.10198A=

Transcript Alleles

HGVS Amino-acid change
ENST00000333213.11:c.644A= MANE Select ENSP00000327487.6:p.Lys215=
ENST00000434205.8:c.341A= ENSP00000406559.4:p.Lys114=
ENST00000545228.3:c.644A= ENSP00000438169.3:p.Lys215=
ENST00000579449.2:n.443A=
ENST00000580013.6:n.847A=
ENST00000583818.2:c.698A= ENSP00000461928.2:n.698A=
ENST00000679370.1:n.1225A=
ENST00000679429.1:c.*102A= ENSP00000505403.1:n.*102A=
ENST00000679443.1:n.713A=
ENST00000679782.1:c.644A= ENSP00000505995.1:p.Lys215=
ENST00000679919.1:n.713A=
ENST00000679928.1:c.*255A= ENSP00000506071.1:n.*255A=
ENST00000680528.1:n.669A=
ENST00000680999.1:c.644A= ENSP00000504984.1:p.Lys215=
ENST00000681282.1:c.673A= ENSP00000506339.1:p.Arg225=
ENST00000333213.10:c.644A= ENSP00000327487.6:p.Lys215=
ENST00000578415.1:c.604A=
ENST00000583173.5:c.458+215A= ENSP00000463619.1:n.458+215A=
ENST00000583818.1:c.593A= ENSP00000461928.1:n.593A=
NM_207346.2:c.644A= NP_997229.2:p.Lys215=
XM_005257229.2:c.644A= XP_005257286.1:p.Lys215=
XM_006721821.2:c.341A= XP_006721884.1:p.Lys114=
XM_011524616.1:c.644A= XP_011522918.1:p.Lys215=
XM_011524617.1:c.644A= XP_011522919.1:p.Lys215=
XM_011524618.1:c.644A= XP_011522920.1:p.Lys215=
XR_243646.2:n.674A=
XM_005257229.4:c.644A= XP_005257286.1:p.Lys215=
XR_243646.4:n.680A=
NM_207346.3:c.644A= MANE Select NP_997229.2:p.Lys215=