Canonical Allele Identifier: CA2275552652

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524492T= , CM000679.2:g.75524492T=	GRCh38
NC_000017.10:g.73520573T= , CM000679.1:g.73520573T=	GRCh37
NC_000017.9:g.71032168T=	NCBI36
NG_013041.1:g.12965T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*80T= MANE Select	ENSP00000327487.6:n.*80T=
ENST00000434205.8:c.*80T=	ENSP00000406559.4:n.*80T=
ENST00000545228.3:c.*160T=	ENSP00000438169.3:n.*160T=
ENST00000577197.2:n.859T=
ENST00000579449.2:n.2401T=
ENST00000580013.6:n.2805T=
ENST00000679370.1:n.3183T=
ENST00000679429.1:c.*1119T=	ENSP00000505403.1:n.*1119T=
ENST00000679443.1:n.1730T=
ENST00000679782.1:c.*360T=	ENSP00000505995.1:n.*360T=
ENST00000679919.1:n.1932T=
ENST00000679928.1:c.*2213T=	ENSP00000506071.1:n.*2213T=
ENST00000680999.1:c.*80T=	ENSP00000504984.1:n.*80T=
ENST00000681282.1:c.*1848T=	ENSP00000506339.1:n.*1848T=
ENST00000333213.10:c.*80T=	ENSP00000327487.6:n.*80T=
ENST00000545228.2:c.938T=
ENST00000577197.1:n.409T=
NM_207346.2:c.*80T=	NP_997229.2:n.*80T=
XM_005257229.2:c.*160T=	XP_005257286.1:n.*160T=
XM_006721821.2:c.*160T=	XP_006721884.1:n.*160T=
XM_011524616.1:c.*160T=	XP_011522918.1:n.*160T=
XM_011524618.1:c.*80T=	XP_011522920.1:n.*80T=
XR_243646.2:n.1893T=
XM_005257229.4:c.*160T=	XP_005257286.1:n.*160T=
XR_243646.4:n.1899T=
NM_207346.3:c.*80T= MANE Select	NP_997229.2:n.*80T=