Canonical Allele Identifier: CA1594977631

Gene: RNF145

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159176646T= , CM000667.2:g.159176646T=	GRCh38
NC_000005.9:g.158603654T= , CM000667.1:g.158603654T=	GRCh37
NC_000005.8:g.158536232T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424310.7:c.607A= MANE Select	ENSP00000409064.2:p.Arg203=
ENST00000274542.6:c.691A=	ENSP00000274542.2:p.Arg231=
ENST00000424310.6:c.607A=	ENSP00000409064.2:p.Arg203=
ENST00000518802.5:c.697A=	ENSP00000430955.1:p.Arg233=
ENST00000519865.5:c.607A=	ENSP00000430397.1:p.Arg203=
ENST00000520638.1:c.649A=	ENSP00000429071.1:p.Arg217=
ENST00000521606.6:c.658A=	ENSP00000430753.2:p.Arg220=
ENST00000611185.4:c.607A=	ENSP00000482720.1:p.Arg203=
NM_001199380.1:c.697A=	NP_001186309.1:p.Arg233=
NM_001199381.1:c.658A=	NP_001186310.1:p.Arg220=
NM_001199382.1:c.649A=	NP_001186311.1:p.Arg217=
NM_001199383.1:c.607A=	NP_001186312.1:p.Arg203=
NM_144726.2:c.691A=	NP_653327.1:p.Arg231=
XM_005265826.3:c.655A=	XP_005265883.1:p.Arg219=
XM_017009138.2:c.607A=	XP_016864627.1:p.Arg203=
XM_024454383.1:c.655A=	XP_024310151.1:p.Arg219=
NM_001199381.2:c.658A=	NP_001186310.1:p.Arg220=
NM_001199383.2:c.607A= MANE Select	NP_001186312.1:p.Arg203=
NM_001199380.2:c.697A=	NP_001186309.1:p.Arg233=
NM_001199382.2:c.649A=	NP_001186311.1:p.Arg217=
NM_144726.3:c.691A=	NP_653327.1:p.Arg231=