Canonical Allele Identifier: CA2275551243

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521823T= , CM000679.2:g.75521823T=	GRCh38
NC_000017.10:g.73517904T= , CM000679.1:g.73517904T=	GRCh37
NC_000017.9:g.71029499T=	NCBI36
NG_013041.1:g.10296T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.742T= MANE Select	ENSP00000327487.6:p.Ser248=
ENST00000434205.8:c.439T=	ENSP00000406559.4:p.Ser147=
ENST00000545228.3:c.742T=	ENSP00000438169.3:p.Ser248=
ENST00000579449.2:n.541T=
ENST00000580013.6:n.945T=
ENST00000583818.2:c.796T=	ENSP00000461928.2:n.796T=
ENST00000679370.1:n.1323T=
ENST00000679429.1:c.*200T=	ENSP00000505403.1:n.*200T=
ENST00000679443.1:n.811T=
ENST00000679782.1:c.742T=	ENSP00000505995.1:p.Ser248=
ENST00000679919.1:n.811T=
ENST00000679928.1:c.*353T=	ENSP00000506071.1:n.*353T=
ENST00000680528.1:n.767T=
ENST00000680999.1:c.742T=	ENSP00000504984.1:p.Ser248=
ENST00000681282.1:c.771T=	ENSP00000506339.1:p.Ser257=
ENST00000333213.10:c.742T=	ENSP00000327487.6:p.Ser248=
ENST00000578415.1:c.702T=
ENST00000583173.5:c.459-184T=	ENSP00000463619.1:n.459-184T=
ENST00000583818.1:c.691T=	ENSP00000461928.1:n.691T=
NM_207346.2:c.742T=	NP_997229.2:p.Ser248=
XM_005257229.2:c.742T=	XP_005257286.1:p.Ser248=
XM_006721821.2:c.439T=	XP_006721884.1:p.Ser147=
XM_011524616.1:c.742T=	XP_011522918.1:p.Ser248=
XM_011524617.1:c.742T=	XP_011522919.1:p.Ser248=
XM_011524618.1:c.742T=	XP_011522920.1:p.Ser248=
XR_243646.2:n.772T=
XM_005257229.4:c.742T=	XP_005257286.1:p.Ser248=
XR_243646.4:n.778T=
NM_207346.3:c.742T= MANE Select	NP_997229.2:p.Ser248=