Canonical Allele Identifier: CA401029468
Gene: TSEN54 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75522009A>T , CM000679.2:g.75522009A>T GRCh38
NC_000017.10:g.73518090A>T , CM000679.1:g.73518090A>T GRCh37
NC_000017.9:g.71029685A>T NCBI36
NG_013041.1:g.10482A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000333213.11:c.928A>T MANE Select ENSP00000327487.6:p.Ser310Cys
ENST00000434205.8:c.625A>T ENSP00000406559.4:p.Ser209Cys
ENST00000545228.3:c.928A>T ENSP00000438169.3:p.Ser310Cys
ENST00000579449.2:n.727A>T
ENST00000580013.6:n.1131A>T
ENST00000679370.1:n.1509A>T
ENST00000679429.1:c.*386A>T ENSP00000505403.1:n.*386A>T
ENST00000679443.1:n.997A>T
ENST00000679782.1:c.928A>T ENSP00000505995.1:p.Ser310Cys
ENST00000679919.1:n.997A>T
ENST00000679928.1:c.*539A>T ENSP00000506071.1:n.*539A>T
ENST00000680528.1:n.953A>T
ENST00000680999.1:c.928A>T ENSP00000504984.1:p.Ser310Cys
ENST00000681282.1:c.*174A>T ENSP00000506339.1:n.*174A>T
ENST00000333213.10:c.928A>T ENSP00000327487.6:p.Ser310Cys
ENST00000545228.2:c.17A>T
ENST00000578415.1:c.888A>T
ENST00000583173.5:c.461A>T ENSP00000463619.1:p.Gln154Leu
NM_207346.2:c.928A>T NP_997229.2:p.Ser310Cys
XM_005257229.2:c.928A>T XP_005257286.1:p.Ser310Cys
XM_006721821.2:c.625A>T XP_006721884.1:p.Ser209Cys
XM_011524616.1:c.928A>T XP_011522918.1:p.Ser310Cys
XM_011524617.1:c.928A>T XP_011522919.1:p.Ser310Cys
XM_011524618.1:c.928A>T XP_011522920.1:p.Ser310Cys
XR_243646.2:n.958A>T
XM_005257229.4:c.928A>T XP_005257286.1:p.Ser310Cys
XR_243646.4:n.964A>T
NM_207346.3:c.928A>T MANE Select NP_997229.2:p.Ser310Cys