Canonical Allele Identifier: CA2275551251

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521841C= , CM000679.2:g.75521841C=	GRCh38
NC_000017.10:g.73517922C= , CM000679.1:g.73517922C=	GRCh37
NC_000017.9:g.71029517C=	NCBI36
NG_013041.1:g.10314C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.760C= MANE Select	ENSP00000327487.6:p.Pro254=
ENST00000434205.8:c.457C=	ENSP00000406559.4:p.Pro153=
ENST00000545228.3:c.760C=	ENSP00000438169.3:p.Pro254=
ENST00000579449.2:n.559C=
ENST00000580013.6:n.963C=
ENST00000583818.2:c.814C=	ENSP00000461928.2:n.814C=
ENST00000679370.1:n.1341C=
ENST00000679429.1:c.*218C=	ENSP00000505403.1:n.*218C=
ENST00000679443.1:n.829C=
ENST00000679782.1:c.760C=	ENSP00000505995.1:p.Pro254=
ENST00000679919.1:n.829C=
ENST00000679928.1:c.*371C=	ENSP00000506071.1:n.*371C=
ENST00000680528.1:n.785C=
ENST00000680999.1:c.760C=	ENSP00000504984.1:p.Pro254=
ENST00000681282.1:c.*6C=	ENSP00000506339.1:n.*6C=
ENST00000333213.10:c.760C=	ENSP00000327487.6:p.Pro254=
ENST00000578415.1:c.720C=
ENST00000583173.5:c.459-166C=	ENSP00000463619.1:n.459-166C=
ENST00000583818.1:c.709C=	ENSP00000461928.1:n.709C=
NM_207346.2:c.760C=	NP_997229.2:p.Pro254=
XM_005257229.2:c.760C=	XP_005257286.1:p.Pro254=
XM_006721821.2:c.457C=	XP_006721884.1:p.Pro153=
XM_011524616.1:c.760C=	XP_011522918.1:p.Pro254=
XM_011524617.1:c.760C=	XP_011522919.1:p.Pro254=
XM_011524618.1:c.760C=	XP_011522920.1:p.Pro254=
XR_243646.2:n.790C=
XM_005257229.4:c.760C=	XP_005257286.1:p.Pro254=
XR_243646.4:n.796C=
NM_207346.3:c.760C= MANE Select	NP_997229.2:p.Pro254=