Canonical Allele Identifier: CA1594977630

Gene: RNF145

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159176643C= , CM000667.2:g.159176643C=	GRCh38
NC_000005.9:g.158603651C= , CM000667.1:g.158603651C=	GRCh37
NC_000005.8:g.158536229C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424310.7:c.610G= MANE Select	ENSP00000409064.2:p.Glu204=
ENST00000274542.6:c.694G=	ENSP00000274542.2:p.Glu232=
ENST00000424310.6:c.610G=	ENSP00000409064.2:p.Glu204=
ENST00000518802.5:c.700G=	ENSP00000430955.1:p.Glu234=
ENST00000519865.5:c.610G=	ENSP00000430397.1:p.Glu204=
ENST00000520638.1:c.652G=	ENSP00000429071.1:p.Glu218=
ENST00000521606.6:c.661G=	ENSP00000430753.2:p.Glu221=
ENST00000611185.4:c.610G=	ENSP00000482720.1:p.Glu204=
NM_001199380.1:c.700G=	NP_001186309.1:p.Glu234=
NM_001199381.1:c.661G=	NP_001186310.1:p.Glu221=
NM_001199382.1:c.652G=	NP_001186311.1:p.Glu218=
NM_001199383.1:c.610G=	NP_001186312.1:p.Glu204=
NM_144726.2:c.694G=	NP_653327.1:p.Glu232=
XM_005265826.3:c.658G=	XP_005265883.1:p.Glu220=
XM_017009138.2:c.610G=	XP_016864627.1:p.Glu204=
XM_024454383.1:c.658G=	XP_024310151.1:p.Glu220=
NM_001199381.2:c.661G=	NP_001186310.1:p.Glu221=
NM_001199383.2:c.610G= MANE Select	NP_001186312.1:p.Glu204=
NM_001199380.2:c.700G=	NP_001186309.1:p.Glu234=
NM_001199382.2:c.652G=	NP_001186311.1:p.Glu218=
NM_144726.3:c.694G=	NP_653327.1:p.Glu232=