Canonical Allele Identifier: CA2275551224

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521793A= , CM000679.2:g.75521793A=	GRCh38
NC_000017.10:g.73517874A= , CM000679.1:g.73517874A=	GRCh37
NC_000017.9:g.71029469A=	NCBI36
NG_013041.1:g.10266A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.712A= MANE Select	ENSP00000327487.6:p.Ser238=
ENST00000434205.8:c.409A=	ENSP00000406559.4:p.Ser137=
ENST00000545228.3:c.712A=	ENSP00000438169.3:p.Ser238=
ENST00000579449.2:n.511A=
ENST00000580013.6:n.915A=
ENST00000583818.2:c.766A=	ENSP00000461928.2:n.766A=
ENST00000679370.1:n.1293A=
ENST00000679429.1:c.*170A=	ENSP00000505403.1:n.*170A=
ENST00000679443.1:n.781A=
ENST00000679782.1:c.712A=	ENSP00000505995.1:p.Ser238=
ENST00000679919.1:n.781A=
ENST00000679928.1:c.*323A=	ENSP00000506071.1:n.*323A=
ENST00000680528.1:n.737A=
ENST00000680999.1:c.712A=	ENSP00000504984.1:p.Ser238=
ENST00000681282.1:c.741A=	ENSP00000506339.1:p.Pro247=
ENST00000333213.10:c.712A=	ENSP00000327487.6:p.Ser238=
ENST00000578415.1:c.672A=
ENST00000583173.5:c.459-214A=	ENSP00000463619.1:n.459-214A=
ENST00000583818.1:c.661A=	ENSP00000461928.1:n.661A=
NM_207346.2:c.712A=	NP_997229.2:p.Ser238=
XM_005257229.2:c.712A=	XP_005257286.1:p.Ser238=
XM_006721821.2:c.409A=	XP_006721884.1:p.Ser137=
XM_011524616.1:c.712A=	XP_011522918.1:p.Ser238=
XM_011524617.1:c.712A=	XP_011522919.1:p.Ser238=
XM_011524618.1:c.712A=	XP_011522920.1:p.Ser238=
XR_243646.2:n.742A=
XM_005257229.4:c.712A=	XP_005257286.1:p.Ser238=
XR_243646.4:n.748A=
NM_207346.3:c.712A= MANE Select	NP_997229.2:p.Ser238=