Canonical Allele Identifier: CA2275551040

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521426A= , CM000679.2:g.75521426A=	GRCh38
NC_000017.10:g.73517507A= , CM000679.1:g.73517507A=	GRCh37
NC_000017.9:g.71029102A=	NCBI36
NG_013041.1:g.9899A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.539A= MANE Select	ENSP00000327487.6:p.Tyr180=
ENST00000434205.8:c.236A=	ENSP00000406559.4:p.Tyr79=
ENST00000545228.3:c.539A=	ENSP00000438169.3:p.Tyr180=
ENST00000579449.2:n.338A=
ENST00000580013.6:n.548A=
ENST00000583818.2:c.593A=	ENSP00000461928.2:n.593A=
ENST00000679370.1:n.926A=
ENST00000679429.1:c.531A=	ENSP00000505403.1:p.Val177=
ENST00000679443.1:n.414A=
ENST00000679782.1:c.539A=	ENSP00000505995.1:p.Tyr180=
ENST00000679919.1:n.414A=
ENST00000679928.1:c.*150A=	ENSP00000506071.1:n.*150A=
ENST00000680528.1:n.564A=
ENST00000680999.1:c.539A=	ENSP00000504984.1:p.Tyr180=
ENST00000681282.1:c.539A=	ENSP00000506339.1:p.Tyr180=
ENST00000333213.10:c.539A=	ENSP00000327487.6:p.Tyr180=
ENST00000578415.1:c.499A=
ENST00000580013.5:n.556A=
ENST00000583173.5:c.374A=	ENSP00000463619.1:p.Tyr125=
ENST00000583818.1:c.488A=	ENSP00000461928.1:n.488A=
NM_207346.2:c.539A=	NP_997229.2:p.Tyr180=
XM_005257229.2:c.539A=	XP_005257286.1:p.Tyr180=
XM_006721821.2:c.236A=	XP_006721884.1:p.Tyr79=
XM_011524616.1:c.539A=	XP_011522918.1:p.Tyr180=
XM_011524617.1:c.539A=	XP_011522919.1:p.Tyr180=
XM_011524618.1:c.539A=	XP_011522920.1:p.Tyr180=
XR_243646.2:n.569A=
XM_005257229.4:c.539A=	XP_005257286.1:p.Tyr180=
XR_243646.4:n.575A=
NM_207346.3:c.539A= MANE Select	NP_997229.2:p.Tyr180=