Canonical Allele Identifier: CA361901138

Gene: RNF145

Linked Data

• MyVariant Identifiers: chr5:g.158603644A>T (hg19) ; chr5:g.159176636A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424310.7:c.617T>A MANE Select	ENSP00000409064.2:p.Val206Asp
ENST00000274542.6:c.701T>A	ENSP00000274542.2:p.Val234Asp
ENST00000424310.6:c.617T>A	ENSP00000409064.2:p.Val206Asp
ENST00000518802.5:c.707T>A	ENSP00000430955.1:p.Val236Asp
ENST00000519865.5:c.617T>A	ENSP00000430397.1:p.Val206Asp
ENST00000520638.1:c.659T>A	ENSP00000429071.1:p.Val220Asp
ENST00000521606.6:c.668T>A	ENSP00000430753.2:p.Val223Asp
ENST00000611185.4:c.617T>A	ENSP00000482720.1:p.Val206Asp
NM_001199380.1:c.707T>A	NP_001186309.1:p.Val236Asp
NM_001199381.1:c.668T>A	NP_001186310.1:p.Val223Asp
NM_001199382.1:c.659T>A	NP_001186311.1:p.Val220Asp
NM_001199383.1:c.617T>A	NP_001186312.1:p.Val206Asp
NM_144726.2:c.701T>A	NP_653327.1:p.Val234Asp
XM_005265826.3:c.665T>A	XP_005265883.1:p.Val222Asp
XM_017009138.2:c.617T>A	XP_016864627.1:p.Val206Asp
XM_024454383.1:c.665T>A	XP_024310151.1:p.Val222Asp
NM_001199381.2:c.668T>A	NP_001186310.1:p.Val223Asp
NM_001199383.2:c.617T>A MANE Select	NP_001186312.1:p.Val206Asp
NM_001199380.2:c.707T>A	NP_001186309.1:p.Val236Asp
NM_001199382.2:c.659T>A	NP_001186311.1:p.Val220Asp
NM_144726.3:c.701T>A	NP_653327.1:p.Val234Asp