Canonical Allele Identifier: CA2275552317
Gene: TSEN54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75523764G= , CM000679.2:g.75523764G= GRCh38
NC_000017.10:g.73519845G= , CM000679.1:g.73519845G= GRCh37
NC_000017.9:g.71031440G= NCBI36
NG_013041.1:g.12237G=

Transcript Alleles

HGVS Amino-acid Change
NM_207346.3:c.1415G= MANE Select NP_997229.2:p.Arg472=
ENST00000333213.11:c.1415G= MANE Select ENSP00000327487.6:p.Arg472=
NM_207346.2:c.1415G= NP_997229.2:p.Arg472=
ENST00000333213.10:c.1415G= ENSP00000327487.6:p.Arg472=
ENST00000434205.8:c.1112G= ENSP00000406559.4:p.Arg371=
ENST00000545228.2:c.692G=
ENST00000545228.3:c.1603G= ENSP00000438169.3:p.Gly535=
ENST00000577197.1:n.163G=
ENST00000577197.2:n.613G=
ENST00000579449.1:n.612G=
ENST00000579449.2:n.2155G=
ENST00000580013.6:n.2559G=
ENST00000679370.1:n.2937G=
ENST00000679429.1:c.*873G= ENSP00000505403.1:n.*873G=
ENST00000679443.1:n.1484G=
ENST00000679782.1:c.*114G= ENSP00000505995.1:n.*114G=
ENST00000679919.1:n.1686G=
ENST00000679928.1:c.*1967G= ENSP00000506071.1:n.*1967G=
ENST00000680528.1:n.2381G=
ENST00000680999.1:c.1628G= ENSP00000504984.1:p.Arg543=
ENST00000681282.1:c.*1602G= ENSP00000506339.1:n.*1602G=
XM_005257229.2:c.1603G= XP_005257286.1:p.Gly535=
XM_005257229.4:c.1603G= XP_005257286.1:p.Gly535=
XM_006721821.2:c.1300G= XP_006721884.1:p.Gly434=
XM_011524616.1:c.1501+429G= XP_011522918.1:n.1501+429G=
XM_011524617.1:c.*12+429G= XP_011522919.1:n.*12+429G=
XM_011524618.1:c.1313+429G= XP_011522920.1:n.1313+429G=
XR_001753015.1:n.88-396C=
XR_001753016.1:n.89-360C=
XR_243646.2:n.1647G=
XR_243646.4:n.1653G=