Canonical Allele Identifier: CA2275551071

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521500T= , CM000679.2:g.75521500T=	GRCh38
NC_000017.10:g.73517581T= , CM000679.1:g.73517581T=	GRCh37
NC_000017.9:g.71029176T=	NCBI36
NG_013041.1:g.9973T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.613T= MANE Select	ENSP00000327487.6:p.Ser205=
ENST00000434205.8:c.310T=	ENSP00000406559.4:p.Ser104=
ENST00000545228.3:c.613T=	ENSP00000438169.3:p.Ser205=
ENST00000579449.2:n.412T=
ENST00000580013.6:n.622T=
ENST00000583818.2:c.667T=	ENSP00000461928.2:n.667T=
ENST00000679370.1:n.1000T=
ENST00000679429.1:c.*71T=	ENSP00000505403.1:n.*71T=
ENST00000679443.1:n.488T=
ENST00000679782.1:c.613T=	ENSP00000505995.1:p.Ser205=
ENST00000679919.1:n.488T=
ENST00000679928.1:c.*224T=	ENSP00000506071.1:n.*224T=
ENST00000680528.1:n.638T=
ENST00000680999.1:c.613T=	ENSP00000504984.1:p.Ser205=
ENST00000681282.1:c.613T=	ENSP00000506339.1:p.Ser205=
ENST00000333213.10:c.613T=	ENSP00000327487.6:p.Ser205=
ENST00000578415.1:c.573T=
ENST00000583173.5:c.448T=	ENSP00000463619.1:p.Ser150=
ENST00000583818.1:c.562T=	ENSP00000461928.1:n.562T=
NM_207346.2:c.613T=	NP_997229.2:p.Ser205=
XM_005257229.2:c.613T=	XP_005257286.1:p.Ser205=
XM_006721821.2:c.310T=	XP_006721884.1:p.Ser104=
XM_011524616.1:c.613T=	XP_011522918.1:p.Ser205=
XM_011524617.1:c.613T=	XP_011522919.1:p.Ser205=
XM_011524618.1:c.613T=	XP_011522920.1:p.Ser205=
XR_243646.2:n.643T=
XM_005257229.4:c.613T=	XP_005257286.1:p.Ser205=
XR_243646.4:n.649T=
NM_207346.3:c.613T= MANE Select	NP_997229.2:p.Ser205=