Canonical Allele Identifier: CA2275552766

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524694T= , CM000679.2:g.75524694T=	GRCh38
NC_000017.10:g.73520775T= , CM000679.1:g.73520775T=	GRCh37
NC_000017.9:g.71032370T=	NCBI36
NG_013041.1:g.13167T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*282T= MANE Select	ENSP00000327487.6:n.*282T=
ENST00000434205.8:c.*282T=	ENSP00000406559.4:n.*282T=
ENST00000577197.2:n.1061T=
ENST00000579449.2:n.2603T=
ENST00000580013.6:n.3007T=
ENST00000679370.1:n.3385T=
ENST00000679429.1:c.*1321T=	ENSP00000505403.1:n.*1321T=
ENST00000679443.1:n.1932T=
ENST00000679782.1:c.*562T=	ENSP00000505995.1:n.*562T=
ENST00000679919.1:n.2134T=
ENST00000679928.1:c.*2415T=	ENSP00000506071.1:n.*2415T=
ENST00000680999.1:c.*282T=	ENSP00000504984.1:n.*282T=
ENST00000681282.1:c.*2050T=	ENSP00000506339.1:n.*2050T=
ENST00000333213.10:c.*282T=	ENSP00000327487.6:n.*282T=
ENST00000577197.1:n.611T=
NM_207346.2:c.*282T=	NP_997229.2:n.*282T=
XM_005257229.2:c.*362T=	XP_005257286.1:n.*362T=
XM_006721821.2:c.*362T=	XP_006721884.1:n.*362T=
XM_011524616.1:c.*362T=	XP_011522918.1:n.*362T=
XM_011524618.1:c.*282T=	XP_011522920.1:n.*282T=
XR_243646.2:n.2095T=
XM_005257229.4:c.*362T=	XP_005257286.1:n.*362T=
XR_243646.4:n.2101T=
NM_207346.3:c.*282T= MANE Select	NP_997229.2:n.*282T=