Canonical Allele Identifier: CA2275551049

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521451C= , CM000679.2:g.75521451C=	GRCh38
NC_000017.10:g.73517532C= , CM000679.1:g.73517532C=	GRCh37
NC_000017.9:g.71029127C=	NCBI36
NG_013041.1:g.9924C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.564C= MANE Select	ENSP00000327487.6:p.Ala188=
ENST00000434205.8:c.261C=	ENSP00000406559.4:p.Ala87=
ENST00000545228.3:c.564C=	ENSP00000438169.3:p.Ala188=
ENST00000579449.2:n.363C=
ENST00000580013.6:n.573C=
ENST00000583818.2:c.618C=	ENSP00000461928.2:n.618C=
ENST00000679370.1:n.951C=
ENST00000679429.1:c.*22C=	ENSP00000505403.1:n.*22C=
ENST00000679443.1:n.439C=
ENST00000679782.1:c.564C=	ENSP00000505995.1:p.Ala188=
ENST00000679919.1:n.439C=
ENST00000679928.1:c.*175C=	ENSP00000506071.1:n.*175C=
ENST00000680528.1:n.589C=
ENST00000680999.1:c.564C=	ENSP00000504984.1:p.Ala188=
ENST00000681282.1:c.564C=	ENSP00000506339.1:p.Ala188=
ENST00000333213.10:c.564C=	ENSP00000327487.6:p.Ala188=
ENST00000578415.1:c.524C=
ENST00000583173.5:c.399C=	ENSP00000463619.1:p.Ala133=
ENST00000583818.1:c.513C=	ENSP00000461928.1:n.513C=
NM_207346.2:c.564C=	NP_997229.2:p.Ala188=
XM_005257229.2:c.564C=	XP_005257286.1:p.Ala188=
XM_006721821.2:c.261C=	XP_006721884.1:p.Ala87=
XM_011524616.1:c.564C=	XP_011522918.1:p.Ala188=
XM_011524617.1:c.564C=	XP_011522919.1:p.Ala188=
XM_011524618.1:c.564C=	XP_011522920.1:p.Ala188=
XR_243646.2:n.594C=
XM_005257229.4:c.564C=	XP_005257286.1:p.Ala188=
XR_243646.4:n.600C=
NM_207346.3:c.564C= MANE Select	NP_997229.2:p.Ala188=