Canonical Allele Identifier: CA361901142
Gene: RNF145 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159176636A>C , CM000667.2:g.159176636A>C GRCh38
NC_000005.9:g.158603644A>C , CM000667.1:g.158603644A>C GRCh37
NC_000005.8:g.158536222A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000424310.7:c.617T>G MANE Select ENSP00000409064.2:p.Val206Gly
ENST00000274542.6:c.701T>G ENSP00000274542.2:p.Val234Gly
ENST00000424310.6:c.617T>G ENSP00000409064.2:p.Val206Gly
ENST00000518802.5:c.707T>G ENSP00000430955.1:p.Val236Gly
ENST00000519865.5:c.617T>G ENSP00000430397.1:p.Val206Gly
ENST00000520638.1:c.659T>G ENSP00000429071.1:p.Val220Gly
ENST00000521606.6:c.668T>G ENSP00000430753.2:p.Val223Gly
ENST00000611185.4:c.617T>G ENSP00000482720.1:p.Val206Gly
NM_001199380.1:c.707T>G NP_001186309.1:p.Val236Gly
NM_001199381.1:c.668T>G NP_001186310.1:p.Val223Gly
NM_001199382.1:c.659T>G NP_001186311.1:p.Val220Gly
NM_001199383.1:c.617T>G NP_001186312.1:p.Val206Gly
NM_144726.2:c.701T>G NP_653327.1:p.Val234Gly
XM_005265826.3:c.665T>G XP_005265883.1:p.Val222Gly
XM_017009138.2:c.617T>G XP_016864627.1:p.Val206Gly
XM_024454383.1:c.665T>G XP_024310151.1:p.Val222Gly
NM_001199381.2:c.668T>G NP_001186310.1:p.Val223Gly
NM_001199383.2:c.617T>G MANE Select NP_001186312.1:p.Val206Gly
NM_001199380.2:c.707T>G NP_001186309.1:p.Val236Gly
NM_001199382.2:c.659T>G NP_001186311.1:p.Val220Gly
NM_144726.3:c.701T>G NP_653327.1:p.Val234Gly