Canonical Allele Identifier: CA2275552659

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524501A= , CM000679.2:g.75524501A=	GRCh38
NC_000017.10:g.73520582A= , CM000679.1:g.73520582A=	GRCh37
NC_000017.9:g.71032177A=	NCBI36
NG_013041.1:g.12974A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*89A= MANE Select	ENSP00000327487.6:n.*89A=
ENST00000434205.8:c.*89A=	ENSP00000406559.4:n.*89A=
ENST00000545228.3:c.*169A=	ENSP00000438169.3:n.*169A=
ENST00000577197.2:n.868A=
ENST00000579449.2:n.2410A=
ENST00000580013.6:n.2814A=
ENST00000679370.1:n.3192A=
ENST00000679429.1:c.*1128A=	ENSP00000505403.1:n.*1128A=
ENST00000679443.1:n.1739A=
ENST00000679782.1:c.*369A=	ENSP00000505995.1:n.*369A=
ENST00000679919.1:n.1941A=
ENST00000679928.1:c.*2222A=	ENSP00000506071.1:n.*2222A=
ENST00000680999.1:c.*89A=	ENSP00000504984.1:n.*89A=
ENST00000681282.1:c.*1857A=	ENSP00000506339.1:n.*1857A=
ENST00000333213.10:c.*89A=	ENSP00000327487.6:n.*89A=
ENST00000545228.2:c.947A=
ENST00000577197.1:n.418A=
NM_207346.2:c.*89A=	NP_997229.2:n.*89A=
XM_005257229.2:c.*169A=	XP_005257286.1:n.*169A=
XM_006721821.2:c.*169A=	XP_006721884.1:n.*169A=
XM_011524616.1:c.*169A=	XP_011522918.1:n.*169A=
XM_011524618.1:c.*89A=	XP_011522920.1:n.*89A=
XR_243646.2:n.1902A=
XM_005257229.4:c.*169A=	XP_005257286.1:n.*169A=
XR_243646.4:n.1908A=
NM_207346.3:c.*89A= MANE Select	NP_997229.2:n.*89A=