Canonical Allele Identifier: CA361901140

Gene: RNF145

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424310.7:c.617T>C MANE Select	ENSP00000409064.2:p.Val206Ala
ENST00000274542.6:c.701T>C	ENSP00000274542.2:p.Val234Ala
ENST00000424310.6:c.617T>C	ENSP00000409064.2:p.Val206Ala
ENST00000518802.5:c.707T>C	ENSP00000430955.1:p.Val236Ala
ENST00000519865.5:c.617T>C	ENSP00000430397.1:p.Val206Ala
ENST00000520638.1:c.659T>C	ENSP00000429071.1:p.Val220Ala
ENST00000521606.6:c.668T>C	ENSP00000430753.2:p.Val223Ala
ENST00000611185.4:c.617T>C	ENSP00000482720.1:p.Val206Ala
NM_001199380.1:c.707T>C	NP_001186309.1:p.Val236Ala
NM_001199381.1:c.668T>C	NP_001186310.1:p.Val223Ala
NM_001199382.1:c.659T>C	NP_001186311.1:p.Val220Ala
NM_001199383.1:c.617T>C	NP_001186312.1:p.Val206Ala
NM_144726.2:c.701T>C	NP_653327.1:p.Val234Ala
XM_005265826.3:c.665T>C	XP_005265883.1:p.Val222Ala
XM_017009138.2:c.617T>C	XP_016864627.1:p.Val206Ala
XM_024454383.1:c.665T>C	XP_024310151.1:p.Val222Ala
NM_001199381.2:c.668T>C	NP_001186310.1:p.Val223Ala
NM_001199383.2:c.617T>C MANE Select	NP_001186312.1:p.Val206Ala
NM_001199380.2:c.707T>C	NP_001186309.1:p.Val236Ala
NM_001199382.2:c.659T>C	NP_001186311.1:p.Val220Ala
NM_144726.3:c.701T>C	NP_653327.1:p.Val234Ala