Canonical Allele Identifier: CA2275552724

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524628A= , CM000679.2:g.75524628A=	GRCh38
NC_000017.10:g.73520709A= , CM000679.1:g.73520709A=	GRCh37
NC_000017.9:g.71032304A=	NCBI36
NG_013041.1:g.13101A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*216A= MANE Select	ENSP00000327487.6:n.*216A=
ENST00000434205.8:c.*216A=	ENSP00000406559.4:n.*216A=
ENST00000545228.3:c.*296A=	ENSP00000438169.3:n.*296A=
ENST00000577197.2:n.995A=
ENST00000579449.2:n.2537A=
ENST00000580013.6:n.2941A=
ENST00000679370.1:n.3319A=
ENST00000679429.1:c.*1255A=	ENSP00000505403.1:n.*1255A=
ENST00000679443.1:n.1866A=
ENST00000679782.1:c.*496A=	ENSP00000505995.1:n.*496A=
ENST00000679919.1:n.2068A=
ENST00000679928.1:c.*2349A=	ENSP00000506071.1:n.*2349A=
ENST00000680999.1:c.*216A=	ENSP00000504984.1:n.*216A=
ENST00000681282.1:c.*1984A=	ENSP00000506339.1:n.*1984A=
ENST00000333213.10:c.*216A=	ENSP00000327487.6:n.*216A=
ENST00000545228.2:c.1074A=
ENST00000577197.1:n.545A=
NM_207346.2:c.*216A=	NP_997229.2:n.*216A=
XM_005257229.2:c.*296A=	XP_005257286.1:n.*296A=
XM_006721821.2:c.*296A=	XP_006721884.1:n.*296A=
XM_011524616.1:c.*296A=	XP_011522918.1:n.*296A=
XM_011524618.1:c.*216A=	XP_011522920.1:n.*216A=
XR_243646.2:n.2029A=
XM_005257229.4:c.*296A=	XP_005257286.1:n.*296A=
XR_243646.4:n.2035A=
NM_207346.3:c.*216A= MANE Select	NP_997229.2:n.*216A=