Canonical Allele Identifier: CA2275551367

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75522028G= , CM000679.2:g.75522028G=	GRCh38
NC_000017.10:g.73518109G= , CM000679.1:g.73518109G=	GRCh37
NC_000017.9:g.71029704G=	NCBI36
NG_013041.1:g.10501G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.947G= MANE Select	ENSP00000327487.6:p.Arg316=
ENST00000434205.8:c.644G=	ENSP00000406559.4:p.Arg215=
ENST00000545228.3:c.947G=	ENSP00000438169.3:p.Arg316=
ENST00000579449.2:n.746G=
ENST00000580013.6:n.1150G=
ENST00000679370.1:n.1528G=
ENST00000679429.1:c.*405G=	ENSP00000505403.1:n.*405G=
ENST00000679443.1:n.1016G=
ENST00000679782.1:c.947G=	ENSP00000505995.1:p.Arg316=
ENST00000679919.1:n.1016G=
ENST00000679928.1:c.*558G=	ENSP00000506071.1:n.*558G=
ENST00000680528.1:n.972G=
ENST00000680999.1:c.947G=	ENSP00000504984.1:p.Arg316=
ENST00000681282.1:c.*193G=	ENSP00000506339.1:n.*193G=
ENST00000333213.10:c.947G=	ENSP00000327487.6:p.Arg316=
ENST00000545228.2:c.36G=
ENST00000578415.1:c.907G=
ENST00000583173.5:c.480G=	ENSP00000463619.1:p.Ala160=
NM_207346.2:c.947G=	NP_997229.2:p.Arg316=
XM_005257229.2:c.947G=	XP_005257286.1:p.Arg316=
XM_006721821.2:c.644G=	XP_006721884.1:p.Arg215=
XM_011524616.1:c.947G=	XP_011522918.1:p.Arg316=
XM_011524617.1:c.947G=	XP_011522919.1:p.Arg316=
XM_011524618.1:c.947G=	XP_011522920.1:p.Arg316=
XR_243646.2:n.977G=
XM_005257229.4:c.947G=	XP_005257286.1:p.Arg316=
XR_243646.4:n.983G=
NM_207346.3:c.947G= MANE Select	NP_997229.2:p.Arg316=