Canonical Allele Identifier: CA2275552707

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524593T= , CM000679.2:g.75524593T=	GRCh38
NC_000017.10:g.73520674T= , CM000679.1:g.73520674T=	GRCh37
NC_000017.9:g.71032269T=	NCBI36
NG_013041.1:g.13066T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*181T= MANE Select	ENSP00000327487.6:n.*181T=
ENST00000434205.8:c.*181T=	ENSP00000406559.4:n.*181T=
ENST00000545228.3:c.*261T=	ENSP00000438169.3:n.*261T=
ENST00000577197.2:n.960T=
ENST00000579449.2:n.2502T=
ENST00000580013.6:n.2906T=
ENST00000679370.1:n.3284T=
ENST00000679429.1:c.*1220T=	ENSP00000505403.1:n.*1220T=
ENST00000679443.1:n.1831T=
ENST00000679782.1:c.*461T=	ENSP00000505995.1:n.*461T=
ENST00000679919.1:n.2033T=
ENST00000679928.1:c.*2314T=	ENSP00000506071.1:n.*2314T=
ENST00000680999.1:c.*181T=	ENSP00000504984.1:n.*181T=
ENST00000681282.1:c.*1949T=	ENSP00000506339.1:n.*1949T=
ENST00000333213.10:c.*181T=	ENSP00000327487.6:n.*181T=
ENST00000545228.2:c.1039T=
ENST00000577197.1:n.510T=
NM_207346.2:c.*181T=	NP_997229.2:n.*181T=
XM_005257229.2:c.*261T=	XP_005257286.1:n.*261T=
XM_006721821.2:c.*261T=	XP_006721884.1:n.*261T=
XM_011524616.1:c.*261T=	XP_011522918.1:n.*261T=
XM_011524618.1:c.*181T=	XP_011522920.1:n.*181T=
XR_243646.2:n.1994T=
XM_005257229.4:c.*261T=	XP_005257286.1:n.*261T=
XR_243646.4:n.2000T=
NM_207346.3:c.*181T= MANE Select	NP_997229.2:n.*181T=