Canonical Allele Identifier: CA2275551262

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521864G= , CM000679.2:g.75521864G=	GRCh38
NC_000017.10:g.73517945G= , CM000679.1:g.73517945G=	GRCh37
NC_000017.9:g.71029540G=	NCBI36
NG_013041.1:g.10337G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.783G= MANE Select	ENSP00000327487.6:p.Leu261=
ENST00000434205.8:c.480G=	ENSP00000406559.4:p.Leu160=
ENST00000545228.3:c.783G=	ENSP00000438169.3:p.Leu261=
ENST00000579449.2:n.582G=
ENST00000580013.6:n.986G=
ENST00000583818.2:c.837G=	ENSP00000461928.2:n.837G=
ENST00000679370.1:n.1364G=
ENST00000679429.1:c.*241G=	ENSP00000505403.1:n.*241G=
ENST00000679443.1:n.852G=
ENST00000679782.1:c.783G=	ENSP00000505995.1:p.Leu261=
ENST00000679919.1:n.852G=
ENST00000679928.1:c.*394G=	ENSP00000506071.1:n.*394G=
ENST00000680528.1:n.808G=
ENST00000680999.1:c.783G=	ENSP00000504984.1:p.Leu261=
ENST00000681282.1:c.*29G=	ENSP00000506339.1:n.*29G=
ENST00000333213.10:c.783G=	ENSP00000327487.6:p.Leu261=
ENST00000578415.1:c.743G=
ENST00000583173.5:c.459-143G=	ENSP00000463619.1:n.459-143G=
ENST00000583818.1:c.732G=	ENSP00000461928.1:n.732G=
NM_207346.2:c.783G=	NP_997229.2:p.Leu261=
XM_005257229.2:c.783G=	XP_005257286.1:p.Leu261=
XM_006721821.2:c.480G=	XP_006721884.1:p.Leu160=
XM_011524616.1:c.783G=	XP_011522918.1:p.Leu261=
XM_011524617.1:c.783G=	XP_011522919.1:p.Leu261=
XM_011524618.1:c.783G=	XP_011522920.1:p.Leu261=
XR_243646.2:n.813G=
XM_005257229.4:c.783G=	XP_005257286.1:p.Leu261=
XR_243646.4:n.819G=
NM_207346.3:c.783G= MANE Select	NP_997229.2:p.Leu261=