Canonical Allele Identifier: CA2275551237

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521813A= , CM000679.2:g.75521813A=	GRCh38
NC_000017.10:g.73517894A= , CM000679.1:g.73517894A=	GRCh37
NC_000017.9:g.71029489A=	NCBI36
NG_013041.1:g.10286A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333213.11:c.732A= MANE Select	ENSP00000327487.6:p.Lys244=
ENST00000434205.8:c.429A=	ENSP00000406559.4:p.Lys143=
ENST00000545228.3:c.732A=	ENSP00000438169.3:p.Lys244=
ENST00000579449.2:n.531A=
ENST00000580013.6:n.935A=
ENST00000583818.2:c.786A=	ENSP00000461928.2:n.786A=
ENST00000679370.1:n.1313A=
ENST00000679429.1:c.*190A=	ENSP00000505403.1:n.*190A=
ENST00000679443.1:n.801A=
ENST00000679782.1:c.732A=	ENSP00000505995.1:p.Lys244=
ENST00000679919.1:n.801A=
ENST00000679928.1:c.*343A=	ENSP00000506071.1:n.*343A=
ENST00000680528.1:n.757A=
ENST00000680999.1:c.732A=	ENSP00000504984.1:p.Lys244=
ENST00000681282.1:c.761A=	ENSP00000506339.1:p.Asn254=
ENST00000333213.10:c.732A=	ENSP00000327487.6:p.Lys244=
ENST00000578415.1:c.692A=
ENST00000583173.5:c.459-194A=	ENSP00000463619.1:n.459-194A=
ENST00000583818.1:c.681A=	ENSP00000461928.1:n.681A=
NM_207346.2:c.732A=	NP_997229.2:p.Lys244=
XM_005257229.2:c.732A=	XP_005257286.1:p.Lys244=
XM_006721821.2:c.429A=	XP_006721884.1:p.Lys143=
XM_011524616.1:c.732A=	XP_011522918.1:p.Lys244=
XM_011524617.1:c.732A=	XP_011522919.1:p.Lys244=
XM_011524618.1:c.732A=	XP_011522920.1:p.Lys244=
XR_243646.2:n.762A=
XM_005257229.4:c.732A=	XP_005257286.1:p.Lys244=
XR_243646.4:n.768A=
NM_207346.3:c.732A= MANE Select	NP_997229.2:p.Lys244=