Canonical Allele Identifier: CA401028334
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75521491A>T , CM000679.2:g.75521491A>T GRCh38
NC_000017.10:g.73517572A>T , CM000679.1:g.73517572A>T GRCh37
NC_000017.9:g.71029167A>T NCBI36
NG_013041.1:g.9964A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.604A>T MANE Select ENSP00000327487.6:p.Arg202Trp
ENST00000434205.8:c.301A>T ENSP00000406559.4:p.Arg101Trp
ENST00000545228.3:c.604A>T ENSP00000438169.3:p.Arg202Trp
ENST00000579449.2:n.403A>T
ENST00000580013.6:n.613A>T
ENST00000583818.2:c.658A>T ENSP00000461928.2:n.658A>T
ENST00000679370.1:n.991A>T
ENST00000679429.1:c.*62A>T ENSP00000505403.1:n.*62A>T
ENST00000679443.1:n.479A>T
ENST00000679782.1:c.604A>T ENSP00000505995.1:p.Arg202Trp
ENST00000679919.1:n.479A>T
ENST00000679928.1:c.*215A>T ENSP00000506071.1:n.*215A>T
ENST00000680528.1:n.629A>T
ENST00000680999.1:c.604A>T ENSP00000504984.1:p.Arg202Trp
ENST00000681282.1:c.604A>T ENSP00000506339.1:p.Arg202Trp
ENST00000333213.10:c.604A>T ENSP00000327487.6:p.Arg202Trp
ENST00000578415.1:c.564A>T
ENST00000583173.5:c.439A>T ENSP00000463619.1:p.Arg147Trp
ENST00000583818.1:c.553A>T ENSP00000461928.1:n.553A>T
NM_207346.2:c.604A>T NP_997229.2:p.Arg202Trp
XM_005257229.2:c.604A>T XP_005257286.1:p.Arg202Trp
XM_006721821.2:c.301A>T XP_006721884.1:p.Arg101Trp
XM_011524616.1:c.604A>T XP_011522918.1:p.Arg202Trp
XM_011524617.1:c.604A>T XP_011522919.1:p.Arg202Trp
XM_011524618.1:c.604A>T XP_011522920.1:p.Arg202Trp
XR_243646.2:n.634A>T
XM_005257229.4:c.604A>T XP_005257286.1:p.Arg202Trp
XR_243646.4:n.640A>T
NM_207346.3:c.604A>T MANE Select NP_997229.2:p.Arg202Trp