Canonical Allele Identifier: CA2275551211

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521772C= , CM000679.2:g.75521772C=	GRCh38
NC_000017.10:g.73517853C= , CM000679.1:g.73517853C=	GRCh37
NC_000017.9:g.71029448C=	NCBI36
NG_013041.1:g.10245C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.691C= MANE Select	ENSP00000327487.6:p.Pro231=
ENST00000434205.8:c.388C=	ENSP00000406559.4:p.Pro130=
ENST00000545228.3:c.691C=	ENSP00000438169.3:p.Pro231=
ENST00000579449.2:n.490C=
ENST00000580013.6:n.894C=
ENST00000583818.2:c.745C=	ENSP00000461928.2:n.745C=
ENST00000679370.1:n.1272C=
ENST00000679429.1:c.*149C=	ENSP00000505403.1:n.*149C=
ENST00000679443.1:n.760C=
ENST00000679782.1:c.691C=	ENSP00000505995.1:p.Pro231=
ENST00000679919.1:n.760C=
ENST00000679928.1:c.*302C=	ENSP00000506071.1:n.*302C=
ENST00000680528.1:n.716C=
ENST00000680999.1:c.691C=	ENSP00000504984.1:p.Pro231=
ENST00000681282.1:c.720C=	ENSP00000506339.1:p.Ala240=
ENST00000333213.10:c.691C=	ENSP00000327487.6:p.Pro231=
ENST00000578415.1:c.651C=
ENST00000583173.5:c.459-235C=	ENSP00000463619.1:n.459-235C=
ENST00000583818.1:c.640C=	ENSP00000461928.1:n.640C=
NM_207346.2:c.691C=	NP_997229.2:p.Pro231=
XM_005257229.2:c.691C=	XP_005257286.1:p.Pro231=
XM_006721821.2:c.388C=	XP_006721884.1:p.Pro130=
XM_011524616.1:c.691C=	XP_011522918.1:p.Pro231=
XM_011524617.1:c.691C=	XP_011522919.1:p.Pro231=
XM_011524618.1:c.691C=	XP_011522920.1:p.Pro231=
XR_243646.2:n.721C=
XM_005257229.4:c.691C=	XP_005257286.1:p.Pro231=
XR_243646.4:n.727C=
NM_207346.3:c.691C= MANE Select	NP_997229.2:p.Pro231=