Canonical Allele Identifier: CA447514180
Gene: RNF145 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158603646C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159176638C>T , CM000667.2:g.159176638C>T GRCh38
NC_000005.9:g.158603646C>T , CM000667.1:g.158603646C>T GRCh37
NC_000005.8:g.158536224C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000424310.7:c.615G>A MANE Select ENSP00000409064.2:p.Leu205=
ENST00000274542.6:c.699G>A ENSP00000274542.2:p.Leu233=
ENST00000424310.6:c.615G>A ENSP00000409064.2:p.Leu205=
ENST00000518802.5:c.705G>A ENSP00000430955.1:p.Leu235=
ENST00000519865.5:c.615G>A ENSP00000430397.1:p.Leu205=
ENST00000520638.1:c.657G>A ENSP00000429071.1:p.Leu219=
ENST00000521606.6:c.666G>A ENSP00000430753.2:p.Leu222=
ENST00000611185.4:c.615G>A ENSP00000482720.1:p.Leu205=
NM_001199380.1:c.705G>A NP_001186309.1:p.Leu235=
NM_001199381.1:c.666G>A NP_001186310.1:p.Leu222=
NM_001199382.1:c.657G>A NP_001186311.1:p.Leu219=
NM_001199383.1:c.615G>A NP_001186312.1:p.Leu205=
NM_144726.2:c.699G>A NP_653327.1:p.Leu233=
XM_005265826.3:c.663G>A XP_005265883.1:p.Leu221=
XM_017009138.2:c.615G>A XP_016864627.1:p.Leu205=
XM_024454383.1:c.663G>A XP_024310151.1:p.Leu221=
NM_001199381.2:c.666G>A NP_001186310.1:p.Leu222=
NM_001199383.2:c.615G>A MANE Select NP_001186312.1:p.Leu205=
NM_001199380.2:c.705G>A NP_001186309.1:p.Leu235=
NM_001199382.2:c.657G>A NP_001186311.1:p.Leu219=
NM_144726.3:c.699G>A NP_653327.1:p.Leu233=