Canonical Allele Identifier: CA502045920
Gene: TSEN54 HGNC NCBI

Linked Data

dbSNP Id: rs1334305972

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75522011C>T , CM000679.2:g.75522011C>T GRCh38
NC_000017.10:g.73518092C>T , CM000679.1:g.73518092C>T GRCh37
NC_000017.9:g.71029687C>T NCBI36
NG_013041.1:g.10484C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333213.11:c.930C>T MANE Select ENSP00000327487.6:p.Ser310=
ENST00000434205.8:c.627C>T ENSP00000406559.4:p.Ser209=
ENST00000545228.3:c.930C>T ENSP00000438169.3:p.Ser310=
ENST00000579449.2:n.729C>T
ENST00000580013.6:n.1133C>T
ENST00000679370.1:n.1511C>T
ENST00000679429.1:c.*388C>T ENSP00000505403.1:n.*388C>T
ENST00000679443.1:n.999C>T
ENST00000679782.1:c.930C>T ENSP00000505995.1:p.Ser310=
ENST00000679919.1:n.999C>T
ENST00000679928.1:c.*541C>T ENSP00000506071.1:n.*541C>T
ENST00000680528.1:n.955C>T
ENST00000680999.1:c.930C>T ENSP00000504984.1:p.Ser310=
ENST00000681282.1:c.*176C>T ENSP00000506339.1:n.*176C>T
ENST00000333213.10:c.930C>T ENSP00000327487.6:p.Ser310=
ENST00000545228.2:c.19C>T
ENST00000578415.1:c.890C>T
ENST00000583173.5:c.463C>T ENSP00000463619.1:p.Pro155Ser
NM_207346.2:c.930C>T NP_997229.2:p.Ser310=
XM_005257229.2:c.930C>T XP_005257286.1:p.Ser310=
XM_006721821.2:c.627C>T XP_006721884.1:p.Ser209=
XM_011524616.1:c.930C>T XP_011522918.1:p.Ser310=
XM_011524617.1:c.930C>T XP_011522919.1:p.Ser310=
XM_011524618.1:c.930C>T XP_011522920.1:p.Ser310=
XR_243646.2:n.960C>T
XM_005257229.4:c.930C>T XP_005257286.1:p.Ser310=
XR_243646.4:n.966C>T
NM_207346.3:c.930C>T MANE Select NP_997229.2:p.Ser310=