Canonical Allele Identifier: CA2275551254

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521848G= , CM000679.2:g.75521848G=	GRCh38
NC_000017.10:g.73517929G= , CM000679.1:g.73517929G=	GRCh37
NC_000017.9:g.71029524G=	NCBI36
NG_013041.1:g.10321G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.767G= MANE Select	ENSP00000327487.6:p.Gly256=
ENST00000434205.8:c.464G=	ENSP00000406559.4:p.Gly155=
ENST00000545228.3:c.767G=	ENSP00000438169.3:p.Gly256=
ENST00000579449.2:n.566G=
ENST00000580013.6:n.970G=
ENST00000583818.2:c.821G=	ENSP00000461928.2:n.821G=
ENST00000679370.1:n.1348G=
ENST00000679429.1:c.*225G=	ENSP00000505403.1:n.*225G=
ENST00000679443.1:n.836G=
ENST00000679782.1:c.767G=	ENSP00000505995.1:p.Gly256=
ENST00000679919.1:n.836G=
ENST00000679928.1:c.*378G=	ENSP00000506071.1:n.*378G=
ENST00000680528.1:n.792G=
ENST00000680999.1:c.767G=	ENSP00000504984.1:p.Gly256=
ENST00000681282.1:c.*13G=	ENSP00000506339.1:n.*13G=
ENST00000333213.10:c.767G=	ENSP00000327487.6:p.Gly256=
ENST00000578415.1:c.727G=
ENST00000583173.5:c.459-159G=	ENSP00000463619.1:n.459-159G=
ENST00000583818.1:c.716G=	ENSP00000461928.1:n.716G=
NM_207346.2:c.767G=	NP_997229.2:p.Gly256=
XM_005257229.2:c.767G=	XP_005257286.1:p.Gly256=
XM_006721821.2:c.464G=	XP_006721884.1:p.Gly155=
XM_011524616.1:c.767G=	XP_011522918.1:p.Gly256=
XM_011524617.1:c.767G=	XP_011522919.1:p.Gly256=
XM_011524618.1:c.767G=	XP_011522920.1:p.Gly256=
XR_243646.2:n.797G=
XM_005257229.4:c.767G=	XP_005257286.1:p.Gly256=
XR_243646.4:n.803G=
NM_207346.3:c.767G= MANE Select	NP_997229.2:p.Gly256=