Canonical Allele Identifier: CA2639822611
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75516836_75516852del , CM000679.2:g.75516836_75516852del GRCh38
NC_000017.10:g.73512917_73512933del , CM000679.1:g.73512917_73512933del GRCh37
NC_000017.9:g.71024512_71024528del NCBI36
NG_013041.1:g.5309_5325del
NG_033152.1:g.3736_3752del

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.147_163del MANE Select ENSP00000327487.6:p.Gln51ProfsTer?
ENST00000434205.8:c.-82-173_-82-157del ENSP00000406559.4:n.-82-173_-82-157del
ENST00000545228.3:c.147_163del ENSP00000438169.3:p.Gln51ProfsTer?
ENST00000579449.2:n.21-173_21-157del
ENST00000580013.6:n.156_172del
ENST00000583818.2:c.147_163del ENSP00000461928.2:p.Gln51ProfsTer?
ENST00000679370.1:n.534_550del
ENST00000679429.1:c.147_163del ENSP00000505403.1:p.Gln51ProfsTer?
ENST00000679443.1:n.22_38del
ENST00000679782.1:c.147_163del ENSP00000505995.1:p.Gln51ProfsTer?
ENST00000679919.1:n.22_38del
ENST00000679928.1:c.147_163del ENSP00000506071.1:p.Gln51ProfsTer?
ENST00000680528.1:n.172_188del
ENST00000680999.1:c.147_163del ENSP00000504984.1:p.Gln51ProfsTer?
ENST00000681282.1:c.147_163del ENSP00000506339.1:p.Gln51ProfsTer?
ENST00000333213.10:c.147_163del ENSP00000327487.6:p.Gln51ProfsTer?
ENST00000434205.7:c.-82-173_-82-157del ENSP00000406559.3:n.-82-173_-82-157del
ENST00000578415.1:c.25_41del
ENST00000580013.5:n.172_188del
ENST00000583173.5:c.57-173_57-157del ENSP00000463619.1:n.57-173_57-157del
ENST00000583454.1:n.182_198del
ENST00000583818.1:c.42_58del ENSP00000461928.1:p.Gln16ProfsTer?
NM_207346.2:c.147_163del NP_997229.2:p.Gln51ProfsTer?
XM_005257229.2:c.147_163del XP_005257286.1:p.Gln51ProfsTer?
XM_006721821.2:c.-157_-141del XP_006721884.1:n.-157_-141del
XM_011524616.1:c.147_163del XP_011522918.1:p.Gln51ProfsTer?
XM_011524617.1:c.147_163del XP_011522919.1:p.Gln51ProfsTer?
XM_011524618.1:c.147_163del XP_011522920.1:p.Gln51ProfsTer?
XR_243646.2:n.177_193del
XM_005257229.4:c.147_163del XP_005257286.1:p.Gln51ProfsTer?
XR_243646.4:n.183_199del
NM_207346.3:c.147_163del MANE Select NP_997229.2:p.Gln51ProfsTer?