Canonical Allele Identifier: CA1594978121

Gene: RNF145

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159177865A= , CM000667.2:g.159177865A=	GRCh38
NC_000005.9:g.158604873A= , CM000667.1:g.158604873A=	GRCh37
NC_000005.8:g.158537451A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424310.7:c.386-998T= MANE Select	ENSP00000409064.2:n.386-998T=
ENST00000274542.6:c.470-998T=	ENSP00000274542.2:n.470-998T=
ENST00000424310.6:c.386-998T=	ENSP00000409064.2:n.386-998T=
ENST00000518802.5:c.476-998T=	ENSP00000430955.1:n.476-998T=
ENST00000519865.5:c.386-998T=	ENSP00000430397.1:n.386-998T=
ENST00000520638.1:c.428-998T=	ENSP00000429071.1:n.428-998T=
ENST00000521606.6:c.437-998T=	ENSP00000430753.2:n.437-998T=
ENST00000611185.4:c.386-998T=	ENSP00000482720.1:n.386-998T=
NM_001199380.1:c.476-998T=	NP_001186309.1:n.476-998T=
NM_001199381.1:c.437-998T=	NP_001186310.1:n.437-998T=
NM_001199382.1:c.428-998T=	NP_001186311.1:n.428-998T=
NM_001199383.1:c.386-998T=	NP_001186312.1:n.386-998T=
NM_144726.2:c.470-998T=	NP_653327.1:n.470-998T=
XM_005265826.3:c.434-998T=	XP_005265883.1:n.434-998T=
XM_017009138.2:c.386-998T=	XP_016864627.1:n.386-998T=
XM_024454383.1:c.434-998T=	XP_024310151.1:n.434-998T=
NM_001199381.2:c.437-998T=	NP_001186310.1:n.437-998T=
NM_001199383.2:c.386-998T= MANE Select	NP_001186312.1:n.386-998T=
NM_001199380.2:c.476-998T=	NP_001186309.1:n.476-998T=
NM_001199382.2:c.428-998T=	NP_001186311.1:n.428-998T=
NM_144726.3:c.470-998T=	NP_653327.1:n.470-998T=