Canonical Allele Identifier: CA2275551067

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521493G= , CM000679.2:g.75521493G=	GRCh38
NC_000017.10:g.73517574G= , CM000679.1:g.73517574G=	GRCh37
NC_000017.9:g.71029169G=	NCBI36
NG_013041.1:g.9966G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.606G= MANE Select	ENSP00000327487.6:p.Arg202=
ENST00000434205.8:c.303G=	ENSP00000406559.4:p.Arg101=
ENST00000545228.3:c.606G=	ENSP00000438169.3:p.Arg202=
ENST00000579449.2:n.405G=
ENST00000580013.6:n.615G=
ENST00000583818.2:c.660G=	ENSP00000461928.2:n.660G=
ENST00000679370.1:n.993G=
ENST00000679429.1:c.*64G=	ENSP00000505403.1:n.*64G=
ENST00000679443.1:n.481G=
ENST00000679782.1:c.606G=	ENSP00000505995.1:p.Arg202=
ENST00000679919.1:n.481G=
ENST00000679928.1:c.*217G=	ENSP00000506071.1:n.*217G=
ENST00000680528.1:n.631G=
ENST00000680999.1:c.606G=	ENSP00000504984.1:p.Arg202=
ENST00000681282.1:c.606G=	ENSP00000506339.1:p.Arg202=
ENST00000333213.10:c.606G=	ENSP00000327487.6:p.Arg202=
ENST00000578415.1:c.566G=
ENST00000583173.5:c.441G=	ENSP00000463619.1:p.Arg147=
ENST00000583818.1:c.555G=	ENSP00000461928.1:n.555G=
NM_207346.2:c.606G=	NP_997229.2:p.Arg202=
XM_005257229.2:c.606G=	XP_005257286.1:p.Arg202=
XM_006721821.2:c.303G=	XP_006721884.1:p.Arg101=
XM_011524616.1:c.606G=	XP_011522918.1:p.Arg202=
XM_011524617.1:c.606G=	XP_011522919.1:p.Arg202=
XM_011524618.1:c.606G=	XP_011522920.1:p.Arg202=
XR_243646.2:n.636G=
XM_005257229.4:c.606G=	XP_005257286.1:p.Arg202=
XR_243646.4:n.642G=
NM_207346.3:c.606G= MANE Select	NP_997229.2:p.Arg202=