Canonical Allele Identifier: CA2275551193

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521736A= , CM000679.2:g.75521736A=	GRCh38
NC_000017.10:g.73517817A= , CM000679.1:g.73517817A=	GRCh37
NC_000017.9:g.71029412A=	NCBI36
NG_013041.1:g.10209A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333213.11:c.655A= MANE Select	ENSP00000327487.6:p.Asn219=
ENST00000434205.8:c.352A=	ENSP00000406559.4:p.Asn118=
ENST00000545228.3:c.655A=	ENSP00000438169.3:p.Asn219=
ENST00000579449.2:n.454A=
ENST00000580013.6:n.858A=
ENST00000583818.2:c.709A=	ENSP00000461928.2:n.709A=
ENST00000679370.1:n.1236A=
ENST00000679429.1:c.*113A=	ENSP00000505403.1:n.*113A=
ENST00000679443.1:n.724A=
ENST00000679782.1:c.655A=	ENSP00000505995.1:p.Asn219=
ENST00000679919.1:n.724A=
ENST00000679928.1:c.*266A=	ENSP00000506071.1:n.*266A=
ENST00000680528.1:n.680A=
ENST00000680999.1:c.655A=	ENSP00000504984.1:p.Asn219=
ENST00000681282.1:c.684A=	ENSP00000506339.1:p.Thr228=
ENST00000333213.10:c.655A=	ENSP00000327487.6:p.Asn219=
ENST00000578415.1:c.615A=
ENST00000583173.5:c.458+226A=	ENSP00000463619.1:n.458+226A=
ENST00000583818.1:c.604A=	ENSP00000461928.1:n.604A=
NM_207346.2:c.655A=	NP_997229.2:p.Asn219=
XM_005257229.2:c.655A=	XP_005257286.1:p.Asn219=
XM_006721821.2:c.352A=	XP_006721884.1:p.Asn118=
XM_011524616.1:c.655A=	XP_011522918.1:p.Asn219=
XM_011524617.1:c.655A=	XP_011522919.1:p.Asn219=
XM_011524618.1:c.655A=	XP_011522920.1:p.Asn219=
XR_243646.2:n.685A=
XM_005257229.4:c.655A=	XP_005257286.1:p.Asn219=
XR_243646.4:n.691A=
NM_207346.3:c.655A= MANE Select	NP_997229.2:p.Asn219=