Canonical Allele Identifier: CA361901208
Gene: RNF145 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159176642T>G , CM000667.2:g.159176642T>G GRCh38
NC_000005.9:g.158603650T>G , CM000667.1:g.158603650T>G GRCh37
NC_000005.8:g.158536228T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000424310.7:c.611A>C MANE Select ENSP00000409064.2:p.Glu204Ala
ENST00000274542.6:c.695A>C ENSP00000274542.2:p.Glu232Ala
ENST00000424310.6:c.611A>C ENSP00000409064.2:p.Glu204Ala
ENST00000518802.5:c.701A>C ENSP00000430955.1:p.Glu234Ala
ENST00000519865.5:c.611A>C ENSP00000430397.1:p.Glu204Ala
ENST00000520638.1:c.653A>C ENSP00000429071.1:p.Glu218Ala
ENST00000521606.6:c.662A>C ENSP00000430753.2:p.Glu221Ala
ENST00000611185.4:c.611A>C ENSP00000482720.1:p.Glu204Ala
NM_001199380.1:c.701A>C NP_001186309.1:p.Glu234Ala
NM_001199381.1:c.662A>C NP_001186310.1:p.Glu221Ala
NM_001199382.1:c.653A>C NP_001186311.1:p.Glu218Ala
NM_001199383.1:c.611A>C NP_001186312.1:p.Glu204Ala
NM_144726.2:c.695A>C NP_653327.1:p.Glu232Ala
XM_005265826.3:c.659A>C XP_005265883.1:p.Glu220Ala
XM_017009138.2:c.611A>C XP_016864627.1:p.Glu204Ala
XM_024454383.1:c.659A>C XP_024310151.1:p.Glu220Ala
NM_001199381.2:c.662A>C NP_001186310.1:p.Glu221Ala
NM_001199383.2:c.611A>C MANE Select NP_001186312.1:p.Glu204Ala
NM_001199380.2:c.701A>C NP_001186309.1:p.Glu234Ala
NM_001199382.2:c.653A>C NP_001186311.1:p.Glu218Ala
NM_144726.3:c.695A>C NP_653327.1:p.Glu232Ala