Canonical Allele Identifier: CA2275552687

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524566G= , CM000679.2:g.75524566G=	GRCh38
NC_000017.10:g.73520647G= , CM000679.1:g.73520647G=	GRCh37
NC_000017.9:g.71032242G=	NCBI36
NG_013041.1:g.13039G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*154G= MANE Select	ENSP00000327487.6:n.*154G=
ENST00000434205.8:c.*154G=	ENSP00000406559.4:n.*154G=
ENST00000545228.3:c.*234G=	ENSP00000438169.3:n.*234G=
ENST00000577197.2:n.933G=
ENST00000579449.2:n.2475G=
ENST00000580013.6:n.2879G=
ENST00000679370.1:n.3257G=
ENST00000679429.1:c.*1193G=	ENSP00000505403.1:n.*1193G=
ENST00000679443.1:n.1804G=
ENST00000679782.1:c.*434G=	ENSP00000505995.1:n.*434G=
ENST00000679919.1:n.2006G=
ENST00000679928.1:c.*2287G=	ENSP00000506071.1:n.*2287G=
ENST00000680999.1:c.*154G=	ENSP00000504984.1:n.*154G=
ENST00000681282.1:c.*1922G=	ENSP00000506339.1:n.*1922G=
ENST00000333213.10:c.*154G=	ENSP00000327487.6:n.*154G=
ENST00000545228.2:c.1012G=
ENST00000577197.1:n.483G=
NM_207346.2:c.*154G=	NP_997229.2:n.*154G=
XM_005257229.2:c.*234G=	XP_005257286.1:n.*234G=
XM_006721821.2:c.*234G=	XP_006721884.1:n.*234G=
XM_011524616.1:c.*234G=	XP_011522918.1:n.*234G=
XM_011524618.1:c.*154G=	XP_011522920.1:n.*154G=
XR_243646.2:n.1967G=
XM_005257229.4:c.*234G=	XP_005257286.1:n.*234G=
XR_243646.4:n.1973G=
NM_207346.3:c.*154G= MANE Select	NP_997229.2:n.*154G=