Canonical Allele Identifier: CA2275552579

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524353G= , CM000679.2:g.75524353G=	GRCh38
NC_000017.10:g.73520434G= , CM000679.1:g.73520434G=	GRCh37
NC_000017.9:g.71032029G=	NCBI36
NG_013041.1:g.12826G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1522G= MANE Select	ENSP00000327487.6:p.Gly508=
ENST00000434205.8:c.1219G=	ENSP00000406559.4:p.Gly407=
ENST00000545228.3:c.*21G=	ENSP00000438169.3:n.*21G=
ENST00000577197.2:n.720G=
ENST00000579449.2:n.2262G=
ENST00000580013.6:n.2666G=
ENST00000679370.1:n.3044G=
ENST00000679429.1:c.*980G=	ENSP00000505403.1:n.*980G=
ENST00000679443.1:n.1591G=
ENST00000679782.1:c.*221G=	ENSP00000505995.1:n.*221G=
ENST00000679919.1:n.1793G=
ENST00000679928.1:c.*2074G=	ENSP00000506071.1:n.*2074G=
ENST00000680528.1:n.2488G=
ENST00000680999.1:c.1735G=	ENSP00000504984.1:p.Gly579=
ENST00000681282.1:c.*1709G=	ENSP00000506339.1:n.*1709G=
ENST00000333213.10:c.1522G=	ENSP00000327487.6:p.Gly508=
ENST00000545228.2:c.799G=
ENST00000577197.1:n.270G=
ENST00000579449.1:n.719G=
NM_207346.2:c.1522G=	NP_997229.2:p.Gly508=
XM_005257229.2:c.*21G=	XP_005257286.1:n.*21G=
XM_006721821.2:c.*21G=	XP_006721884.1:n.*21G=
XM_011524616.1:c.*21G=	XP_011522918.1:n.*21G=
XM_011524618.1:c.1405G=	XP_011522920.1:p.Gly469=
XR_243646.2:n.1754G=
XM_005257229.4:c.*21G=	XP_005257286.1:n.*21G=
XR_001753015.1:n.45C=
XR_001753016.1:n.46C=
XR_243646.4:n.1760G=
NM_207346.3:c.1522G= MANE Select	NP_997229.2:p.Gly508=