Canonical Allele Identifier: CA2275549713

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75519024T= , CM000679.2:g.75519024T=	GRCh38
NC_000017.10:g.73515105T= , CM000679.1:g.73515105T=	GRCh37
NC_000017.9:g.71026700T=	NCBI36
NG_013041.1:g.7497T=
NG_033152.1:g.1560A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.498T= MANE Select	ENSP00000327487.6:p.Tyr166=
ENST00000434205.8:c.195T=	ENSP00000406559.4:p.Tyr65=
ENST00000545228.3:c.498T=	ENSP00000438169.3:p.Tyr166=
ENST00000579449.2:n.297T=
ENST00000580013.6:n.507T=
ENST00000583818.2:c.498T=	ENSP00000461928.2:p.Tyr166=
ENST00000679370.1:n.885T=
ENST00000679429.1:c.490T=	ENSP00000505403.1:p.Cys164=
ENST00000679443.1:n.373T=
ENST00000679782.1:c.498T=	ENSP00000505995.1:p.Tyr166=
ENST00000679919.1:n.373T=
ENST00000679928.1:c.498T=	ENSP00000506071.1:p.Tyr166=
ENST00000680528.1:n.523T=
ENST00000680999.1:c.498T=	ENSP00000504984.1:p.Tyr166=
ENST00000681282.1:c.498T=	ENSP00000506339.1:p.Tyr166=
ENST00000333213.10:c.498T=	ENSP00000327487.6:p.Tyr166=
ENST00000434205.7:c.195T=	ENSP00000406559.3:p.Tyr65=
ENST00000578415.1:c.458T=
ENST00000580013.5:n.515T=
ENST00000583173.5:c.333T=	ENSP00000463619.1:p.Tyr111=
ENST00000583818.1:c.393T=	ENSP00000461928.1:p.Tyr131=
NM_207346.2:c.498T=	NP_997229.2:p.Tyr166=
XM_005257229.2:c.498T=	XP_005257286.1:p.Tyr166=
XM_006721821.2:c.195T=	XP_006721884.1:p.Tyr65=
XM_011524616.1:c.498T=	XP_011522918.1:p.Tyr166=
XM_011524617.1:c.498T=	XP_011522919.1:p.Tyr166=
XM_011524618.1:c.498T=	XP_011522920.1:p.Tyr166=
XR_243646.2:n.528T=
XM_005257229.4:c.498T=	XP_005257286.1:p.Tyr166=
XR_243646.4:n.534T=
NM_207346.3:c.498T= MANE Select	NP_997229.2:p.Tyr166=