Canonical Allele Identifier: CA2275551178

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521699C= , CM000679.2:g.75521699C=	GRCh38
NC_000017.10:g.73517780C= , CM000679.1:g.73517780C=	GRCh37
NC_000017.9:g.71029375C=	NCBI36
NG_013041.1:g.10172C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.624-6C= MANE Select	ENSP00000327487.6:n.624-6C=
ENST00000434205.8:c.321-6C=	ENSP00000406559.4:n.321-6C=
ENST00000545228.3:c.624-6C=	ENSP00000438169.3:n.624-6C=
ENST00000579449.2:n.423-6C=
ENST00000580013.6:n.821C=
ENST00000583818.2:c.678-6C=	ENSP00000461928.2:n.678-6C=
ENST00000679370.1:n.1199C=
ENST00000679429.1:c.*82-6C=	ENSP00000505403.1:n.*82-6C=
ENST00000679443.1:n.687C=
ENST00000679782.1:c.624-6C=	ENSP00000505995.1:n.624-6C=
ENST00000679919.1:n.687C=
ENST00000679928.1:c.*235-6C=	ENSP00000506071.1:n.*235-6C=
ENST00000680528.1:n.649-6C=
ENST00000680999.1:c.624-6C=	ENSP00000504984.1:n.624-6C=
ENST00000681282.1:c.647C=	ENSP00000506339.1:p.Pro216=
ENST00000333213.10:c.624-6C=	ENSP00000327487.6:n.624-6C=
ENST00000578415.1:c.584-6C=
ENST00000583173.5:c.458+189C=	ENSP00000463619.1:n.458+189C=
ENST00000583818.1:c.573-6C=	ENSP00000461928.1:n.573-6C=
NM_207346.2:c.624-6C=	NP_997229.2:n.624-6C=
XM_005257229.2:c.624-6C=	XP_005257286.1:n.624-6C=
XM_006721821.2:c.321-6C=	XP_006721884.1:n.321-6C=
XM_011524616.1:c.624-6C=	XP_011522918.1:n.624-6C=
XM_011524617.1:c.624-6C=	XP_011522919.1:n.624-6C=
XM_011524618.1:c.624-6C=	XP_011522920.1:n.624-6C=
XR_243646.2:n.654-6C=
XM_005257229.4:c.624-6C=	XP_005257286.1:n.624-6C=
XR_243646.4:n.660-6C=
NM_207346.3:c.624-6C= MANE Select	NP_997229.2:n.624-6C=