Canonical Allele Identifier: CA2275552683

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524561A= , CM000679.2:g.75524561A=	GRCh38
NC_000017.10:g.73520642A= , CM000679.1:g.73520642A=	GRCh37
NC_000017.9:g.71032237A=	NCBI36
NG_013041.1:g.13034A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*149A= MANE Select	ENSP00000327487.6:n.*149A=
ENST00000434205.8:c.*149A=	ENSP00000406559.4:n.*149A=
ENST00000545228.3:c.*229A=	ENSP00000438169.3:n.*229A=
ENST00000577197.2:n.928A=
ENST00000579449.2:n.2470A=
ENST00000580013.6:n.2874A=
ENST00000679370.1:n.3252A=
ENST00000679429.1:c.*1188A=	ENSP00000505403.1:n.*1188A=
ENST00000679443.1:n.1799A=
ENST00000679782.1:c.*429A=	ENSP00000505995.1:n.*429A=
ENST00000679919.1:n.2001A=
ENST00000679928.1:c.*2282A=	ENSP00000506071.1:n.*2282A=
ENST00000680999.1:c.*149A=	ENSP00000504984.1:n.*149A=
ENST00000681282.1:c.*1917A=	ENSP00000506339.1:n.*1917A=
ENST00000333213.10:c.*149A=	ENSP00000327487.6:n.*149A=
ENST00000545228.2:c.1007A=
ENST00000577197.1:n.478A=
NM_207346.2:c.*149A=	NP_997229.2:n.*149A=
XM_005257229.2:c.*229A=	XP_005257286.1:n.*229A=
XM_006721821.2:c.*229A=	XP_006721884.1:n.*229A=
XM_011524616.1:c.*229A=	XP_011522918.1:n.*229A=
XM_011524618.1:c.*149A=	XP_011522920.1:n.*149A=
XR_243646.2:n.1962A=
XM_005257229.4:c.*229A=	XP_005257286.1:n.*229A=
XR_243646.4:n.1968A=
NM_207346.3:c.*149A= MANE Select	NP_997229.2:n.*149A=