Canonical Allele Identifier: CA401026942
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516761C>A , CM000679.2:g.75516761C>A GRCh38
NC_000017.10:g.73512842C>A , CM000679.1:g.73512842C>A GRCh37
NC_000017.9:g.71024437C>A NCBI36
NG_013041.1:g.5234C>A
NG_033152.1:g.3823G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.72C>A MANE Select ENSP00000327487.6:p.Phe24Leu
ENST00000434205.8:c.-82-248C>A ENSP00000406559.4:n.-82-248C>A
ENST00000545228.3:c.72C>A ENSP00000438169.3:p.Phe24Leu
ENST00000579449.2:n.20+145C>A
ENST00000580013.6:n.81C>A
ENST00000583818.2:c.72C>A ENSP00000461928.2:p.Phe24Leu
ENST00000679370.1:n.459C>A
ENST00000679429.1:c.72C>A ENSP00000505403.1:p.Phe24Leu
ENST00000679782.1:c.72C>A ENSP00000505995.1:p.Phe24Leu
ENST00000679928.1:c.72C>A ENSP00000506071.1:p.Phe24Leu
ENST00000680528.1:n.97C>A
ENST00000680999.1:c.72C>A ENSP00000504984.1:p.Phe24Leu
ENST00000681282.1:c.72C>A ENSP00000506339.1:p.Phe24Leu
ENST00000333213.10:c.72C>A ENSP00000327487.6:p.Phe24Leu
ENST00000434205.7:c.-82-248C>A ENSP00000406559.3:n.-82-248C>A
ENST00000580013.5:n.97C>A
ENST00000583173.5:c.56+145C>A ENSP00000463619.1:n.56+145C>A
ENST00000583454.1:n.107C>A
NM_207346.2:c.72C>A NP_997229.2:p.Phe24Leu
XM_005257229.2:c.72C>A XP_005257286.1:p.Phe24Leu
XM_006721821.2:c.-232C>A XP_006721884.1:n.-232C>A
XM_011524616.1:c.72C>A XP_011522918.1:p.Phe24Leu
XM_011524617.1:c.72C>A XP_011522919.1:p.Phe24Leu
XM_011524618.1:c.72C>A XP_011522920.1:p.Phe24Leu
XR_243646.2:n.102C>A
XM_005257229.4:c.72C>A XP_005257286.1:p.Phe24Leu
XR_243646.4:n.108C>A
NM_207346.3:c.72C>A MANE Select NP_997229.2:p.Phe24Leu