Canonical Allele Identifier: CA2275551229

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521801C= , CM000679.2:g.75521801C=	GRCh38
NC_000017.10:g.73517882C= , CM000679.1:g.73517882C=	GRCh37
NC_000017.9:g.71029477C=	NCBI36
NG_013041.1:g.10274C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.720C= MANE Select	ENSP00000327487.6:p.Cys240=
ENST00000434205.8:c.417C=	ENSP00000406559.4:p.Cys139=
ENST00000545228.3:c.720C=	ENSP00000438169.3:p.Cys240=
ENST00000579449.2:n.519C=
ENST00000580013.6:n.923C=
ENST00000583818.2:c.774C=	ENSP00000461928.2:n.774C=
ENST00000679370.1:n.1301C=
ENST00000679429.1:c.*178C=	ENSP00000505403.1:n.*178C=
ENST00000679443.1:n.789C=
ENST00000679782.1:c.720C=	ENSP00000505995.1:p.Cys240=
ENST00000679919.1:n.789C=
ENST00000679928.1:c.*331C=	ENSP00000506071.1:n.*331C=
ENST00000680528.1:n.745C=
ENST00000680999.1:c.720C=	ENSP00000504984.1:p.Cys240=
ENST00000681282.1:c.749C=	ENSP00000506339.1:p.Ala250=
ENST00000333213.10:c.720C=	ENSP00000327487.6:p.Cys240=
ENST00000578415.1:c.680C=
ENST00000583173.5:c.459-206C=	ENSP00000463619.1:n.459-206C=
ENST00000583818.1:c.669C=	ENSP00000461928.1:n.669C=
NM_207346.2:c.720C=	NP_997229.2:p.Cys240=
XM_005257229.2:c.720C=	XP_005257286.1:p.Cys240=
XM_006721821.2:c.417C=	XP_006721884.1:p.Cys139=
XM_011524616.1:c.720C=	XP_011522918.1:p.Cys240=
XM_011524617.1:c.720C=	XP_011522919.1:p.Cys240=
XM_011524618.1:c.720C=	XP_011522920.1:p.Cys240=
XR_243646.2:n.750C=
XM_005257229.4:c.720C=	XP_005257286.1:p.Cys240=
XR_243646.4:n.756C=
NM_207346.3:c.720C= MANE Select	NP_997229.2:p.Cys240=