Canonical Allele Identifier: CA2639824996
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75518935_75518936insC , CM000679.2:g.75518935_75518936insC GRCh38
NC_000017.10:g.73515016_73515017insC , CM000679.1:g.73515016_73515017insC GRCh37
NC_000017.9:g.71026611_71026612insC NCBI36
NG_013041.1:g.7408_7409insC
NG_033152.1:g.1648_1649insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.469-60_469-59insC MANE Select ENSP00000327487.6:n.469-60_469-59insC
ENST00000434205.8:c.166-60_166-59insC ENSP00000406559.4:n.166-60_166-59insC
ENST00000545228.3:c.469-60_469-59insC ENSP00000438169.3:n.469-60_469-59insC
ENST00000579449.2:n.268-60_268-59insC
ENST00000580013.6:n.478-60_478-59insC
ENST00000583818.2:c.469-60_469-59insC ENSP00000461928.2:n.469-60_469-59insC
ENST00000679370.1:n.856-60_856-59insC
ENST00000679429.1:c.469-68_469-67insC ENSP00000505403.1:n.469-68_469-67insC
ENST00000679443.1:n.344-60_344-59insC
ENST00000679782.1:c.469-60_469-59insC ENSP00000505995.1:n.469-60_469-59insC
ENST00000679919.1:n.344-60_344-59insC
ENST00000679928.1:c.469-60_469-59insC ENSP00000506071.1:n.469-60_469-59insC
ENST00000680528.1:n.494-60_494-59insC
ENST00000680999.1:c.469-60_469-59insC ENSP00000504984.1:n.469-60_469-59insC
ENST00000681282.1:c.469-60_469-59insC ENSP00000506339.1:n.469-60_469-59insC
ENST00000333213.10:c.469-60_469-59insC ENSP00000327487.6:n.469-60_469-59insC
ENST00000434205.7:c.166-60_166-59insC ENSP00000406559.3:n.166-60_166-59insC
ENST00000578415.1:c.429-60_429-59insC
ENST00000580013.5:n.494-68_494-67insC
ENST00000583173.5:c.304-60_304-59insC ENSP00000463619.1:n.304-60_304-59insC
ENST00000583818.1:c.364-60_364-59insC ENSP00000461928.1:n.364-60_364-59insC
NM_207346.2:c.469-60_469-59insC NP_997229.2:n.469-60_469-59insC
XM_005257229.2:c.469-60_469-59insC XP_005257286.1:n.469-60_469-59insC
XM_006721821.2:c.166-60_166-59insC XP_006721884.1:n.166-60_166-59insC
XM_011524616.1:c.469-60_469-59insC XP_011522918.1:n.469-60_469-59insC
XM_011524617.1:c.469-60_469-59insC XP_011522919.1:n.469-60_469-59insC
XM_011524618.1:c.469-60_469-59insC XP_011522920.1:n.469-60_469-59insC
XR_243646.2:n.499-60_499-59insC
XM_005257229.4:c.469-60_469-59insC XP_005257286.1:n.469-60_469-59insC
XR_243646.4:n.505-60_505-59insC
NM_207346.3:c.469-60_469-59insC MANE Select NP_997229.2:n.469-60_469-59insC