Canonical Allele Identifier: CA2275551279

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521890C= , CM000679.2:g.75521890C=	GRCh38
NC_000017.10:g.73517971C= , CM000679.1:g.73517971C=	GRCh37
NC_000017.9:g.71029566C=	NCBI36
NG_013041.1:g.10363C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.809C= MANE Select	ENSP00000327487.6:p.Pro270=
ENST00000434205.8:c.506C=	ENSP00000406559.4:p.Pro169=
ENST00000545228.3:c.809C=	ENSP00000438169.3:p.Pro270=
ENST00000579449.2:n.608C=
ENST00000580013.6:n.1012C=
ENST00000583818.2:c.863C=	ENSP00000461928.2:n.863C=
ENST00000679370.1:n.1390C=
ENST00000679429.1:c.*267C=	ENSP00000505403.1:n.*267C=
ENST00000679443.1:n.878C=
ENST00000679782.1:c.809C=	ENSP00000505995.1:p.Pro270=
ENST00000679919.1:n.878C=
ENST00000679928.1:c.*420C=	ENSP00000506071.1:n.*420C=
ENST00000680528.1:n.834C=
ENST00000680999.1:c.809C=	ENSP00000504984.1:p.Pro270=
ENST00000681282.1:c.*55C=	ENSP00000506339.1:n.*55C=
ENST00000333213.10:c.809C=	ENSP00000327487.6:p.Pro270=
ENST00000578415.1:c.769C=
ENST00000583173.5:c.459-117C=	ENSP00000463619.1:n.459-117C=
ENST00000583818.1:c.758C=	ENSP00000461928.1:n.758C=
NM_207346.2:c.809C=	NP_997229.2:p.Pro270=
XM_005257229.2:c.809C=	XP_005257286.1:p.Pro270=
XM_006721821.2:c.506C=	XP_006721884.1:p.Pro169=
XM_011524616.1:c.809C=	XP_011522918.1:p.Pro270=
XM_011524617.1:c.809C=	XP_011522919.1:p.Pro270=
XM_011524618.1:c.809C=	XP_011522920.1:p.Pro270=
XR_243646.2:n.839C=
XM_005257229.4:c.809C=	XP_005257286.1:p.Pro270=
XR_243646.4:n.845C=
NM_207346.3:c.809C= MANE Select	NP_997229.2:p.Pro270=