Canonical Allele Identifier: CA2275552741

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524654G= , CM000679.2:g.75524654G=	GRCh38
NC_000017.10:g.73520735G= , CM000679.1:g.73520735G=	GRCh37
NC_000017.9:g.71032330G=	NCBI36
NG_013041.1:g.13127G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*242G= MANE Select	ENSP00000327487.6:n.*242G=
ENST00000434205.8:c.*242G=	ENSP00000406559.4:n.*242G=
ENST00000545228.3:c.*322G=	ENSP00000438169.3:n.*322G=
ENST00000577197.2:n.1021G=
ENST00000579449.2:n.2563G=
ENST00000580013.6:n.2967G=
ENST00000679370.1:n.3345G=
ENST00000679429.1:c.*1281G=	ENSP00000505403.1:n.*1281G=
ENST00000679443.1:n.1892G=
ENST00000679782.1:c.*522G=	ENSP00000505995.1:n.*522G=
ENST00000679919.1:n.2094G=
ENST00000679928.1:c.*2375G=	ENSP00000506071.1:n.*2375G=
ENST00000680999.1:c.*242G=	ENSP00000504984.1:n.*242G=
ENST00000681282.1:c.*2010G=	ENSP00000506339.1:n.*2010G=
ENST00000333213.10:c.*242G=	ENSP00000327487.6:n.*242G=
ENST00000545228.2:c.1100G=
ENST00000577197.1:n.571G=
NM_207346.2:c.*242G=	NP_997229.2:n.*242G=
XM_005257229.2:c.*322G=	XP_005257286.1:n.*322G=
XM_006721821.2:c.*322G=	XP_006721884.1:n.*322G=
XM_011524616.1:c.*322G=	XP_011522918.1:n.*322G=
XM_011524618.1:c.*242G=	XP_011522920.1:n.*242G=
XR_243646.2:n.2055G=
XM_005257229.4:c.*322G=	XP_005257286.1:n.*322G=
XR_243646.4:n.2061G=
NM_207346.3:c.*242G= MANE Select	NP_997229.2:n.*242G=