Canonical Allele Identifier: CA2275552753

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524678C= , CM000679.2:g.75524678C=	GRCh38
NC_000017.10:g.73520759C= , CM000679.1:g.73520759C=	GRCh37
NC_000017.9:g.71032354C=	NCBI36
NG_013041.1:g.13151C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*266C= MANE Select	ENSP00000327487.6:n.*266C=
ENST00000434205.8:c.*266C=	ENSP00000406559.4:n.*266C=
ENST00000545228.3:c.*346C=	ENSP00000438169.3:n.*346C=
ENST00000577197.2:n.1045C=
ENST00000579449.2:n.2587C=
ENST00000580013.6:n.2991C=
ENST00000679370.1:n.3369C=
ENST00000679429.1:c.*1305C=	ENSP00000505403.1:n.*1305C=
ENST00000679443.1:n.1916C=
ENST00000679782.1:c.*546C=	ENSP00000505995.1:n.*546C=
ENST00000679919.1:n.2118C=
ENST00000679928.1:c.*2399C=	ENSP00000506071.1:n.*2399C=
ENST00000680999.1:c.*266C=	ENSP00000504984.1:n.*266C=
ENST00000681282.1:c.*2034C=	ENSP00000506339.1:n.*2034C=
ENST00000333213.10:c.*266C=	ENSP00000327487.6:n.*266C=
ENST00000545228.2:c.1124C=
ENST00000577197.1:n.595C=
NM_207346.2:c.*266C=	NP_997229.2:n.*266C=
XM_005257229.2:c.*346C=	XP_005257286.1:n.*346C=
XM_006721821.2:c.*346C=	XP_006721884.1:n.*346C=
XM_011524616.1:c.*346C=	XP_011522918.1:n.*346C=
XM_011524618.1:c.*266C=	XP_011522920.1:n.*266C=
XR_243646.2:n.2079C=
XM_005257229.4:c.*346C=	XP_005257286.1:n.*346C=
XR_243646.4:n.2085C=
NM_207346.3:c.*266C= MANE Select	NP_997229.2:n.*266C=