Canonical Allele Identifier: CA502046296

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73518149G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75522068G>T , CM000679.2:g.75522068G>T	GRCh38
NC_000017.10:g.73518149G>T , CM000679.1:g.73518149G>T	GRCh37
NC_000017.9:g.71029744G>T	NCBI36
NG_013041.1:g.10541G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.987G>T MANE Select	ENSP00000327487.6:p.Gly329=
ENST00000434205.8:c.684G>T	ENSP00000406559.4:p.Gly228=
ENST00000545228.3:c.987G>T	ENSP00000438169.3:p.Gly329=
ENST00000579449.2:n.786G>T
ENST00000580013.6:n.1190G>T
ENST00000679370.1:n.1568G>T
ENST00000679429.1:c.*445G>T	ENSP00000505403.1:n.*445G>T
ENST00000679443.1:n.1056G>T
ENST00000679782.1:c.987G>T	ENSP00000505995.1:p.Gly329=
ENST00000679919.1:n.1056G>T
ENST00000679928.1:c.*598G>T	ENSP00000506071.1:n.*598G>T
ENST00000680528.1:n.1012G>T
ENST00000680999.1:c.987G>T	ENSP00000504984.1:p.Gly329=
ENST00000681282.1:c.*233G>T	ENSP00000506339.1:n.*233G>T
ENST00000333213.10:c.987G>T	ENSP00000327487.6:p.Gly329=
ENST00000545228.2:c.76G>T
ENST00000578415.1:c.947G>T
ENST00000583173.5:c.520G>T	ENSP00000463619.1:p.Ala174Ser
NM_207346.2:c.987G>T	NP_997229.2:p.Gly329=
XM_005257229.2:c.987G>T	XP_005257286.1:p.Gly329=
XM_006721821.2:c.684G>T	XP_006721884.1:p.Gly228=
XM_011524616.1:c.987G>T	XP_011522918.1:p.Gly329=
XM_011524617.1:c.987G>T	XP_011522919.1:p.Gly329=
XM_011524618.1:c.987G>T	XP_011522920.1:p.Gly329=
XR_243646.2:n.1017G>T
XM_005257229.4:c.987G>T	XP_005257286.1:p.Gly329=
XR_243646.4:n.1023G>T
NM_207346.3:c.987G>T MANE Select	NP_997229.2:p.Gly329=