Canonical Allele Identifier: CA361901190

Gene: RNF145

Linked Data

• MyVariant Identifiers: chr5:g.158603650T>A (hg19) ; chr5:g.159176642T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424310.7:c.611A>T MANE Select	ENSP00000409064.2:p.Glu204Val
ENST00000274542.6:c.695A>T	ENSP00000274542.2:p.Glu232Val
ENST00000424310.6:c.611A>T	ENSP00000409064.2:p.Glu204Val
ENST00000518802.5:c.701A>T	ENSP00000430955.1:p.Glu234Val
ENST00000519865.5:c.611A>T	ENSP00000430397.1:p.Glu204Val
ENST00000520638.1:c.653A>T	ENSP00000429071.1:p.Glu218Val
ENST00000521606.6:c.662A>T	ENSP00000430753.2:p.Glu221Val
ENST00000611185.4:c.611A>T	ENSP00000482720.1:p.Glu204Val
NM_001199380.1:c.701A>T	NP_001186309.1:p.Glu234Val
NM_001199381.1:c.662A>T	NP_001186310.1:p.Glu221Val
NM_001199382.1:c.653A>T	NP_001186311.1:p.Glu218Val
NM_001199383.1:c.611A>T	NP_001186312.1:p.Glu204Val
NM_144726.2:c.695A>T	NP_653327.1:p.Glu232Val
XM_005265826.3:c.659A>T	XP_005265883.1:p.Glu220Val
XM_017009138.2:c.611A>T	XP_016864627.1:p.Glu204Val
XM_024454383.1:c.659A>T	XP_024310151.1:p.Glu220Val
NM_001199381.2:c.662A>T	NP_001186310.1:p.Glu221Val
NM_001199383.2:c.611A>T MANE Select	NP_001186312.1:p.Glu204Val
NM_001199380.2:c.701A>T	NP_001186309.1:p.Glu234Val
NM_001199382.2:c.653A>T	NP_001186311.1:p.Glu218Val
NM_144726.3:c.695A>T	NP_653327.1:p.Glu232Val