Canonical Allele Identifier: CA361901129

Gene: RNF145

Linked Data

• MyVariant Identifiers: chr5:g.158603642G>C (hg19) ; chr5:g.159176634G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159176634G>C , CM000667.2:g.159176634G>C	GRCh38
NC_000005.9:g.158603642G>C , CM000667.1:g.158603642G>C	GRCh37
NC_000005.8:g.158536220G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424310.7:c.619C>G MANE Select	ENSP00000409064.2:p.Gln207Glu
ENST00000274542.6:c.703C>G	ENSP00000274542.2:p.Gln235Glu
ENST00000424310.6:c.619C>G	ENSP00000409064.2:p.Gln207Glu
ENST00000518802.5:c.709C>G	ENSP00000430955.1:p.Gln237Glu
ENST00000519865.5:c.619C>G	ENSP00000430397.1:p.Gln207Glu
ENST00000520638.1:c.661C>G	ENSP00000429071.1:p.Gln221Glu
ENST00000521606.6:c.670C>G	ENSP00000430753.2:p.Gln224Glu
ENST00000611185.4:c.619C>G	ENSP00000482720.1:p.Gln207Glu
NM_001199380.1:c.709C>G	NP_001186309.1:p.Gln237Glu
NM_001199381.1:c.670C>G	NP_001186310.1:p.Gln224Glu
NM_001199382.1:c.661C>G	NP_001186311.1:p.Gln221Glu
NM_001199383.1:c.619C>G	NP_001186312.1:p.Gln207Glu
NM_144726.2:c.703C>G	NP_653327.1:p.Gln235Glu
XM_005265826.3:c.667C>G	XP_005265883.1:p.Gln223Glu
XM_017009138.2:c.619C>G	XP_016864627.1:p.Gln207Glu
XM_024454383.1:c.667C>G	XP_024310151.1:p.Gln223Glu
NM_001199381.2:c.670C>G	NP_001186310.1:p.Gln224Glu
NM_001199383.2:c.619C>G MANE Select	NP_001186312.1:p.Gln207Glu
NM_001199380.2:c.709C>G	NP_001186309.1:p.Gln237Glu
NM_001199382.2:c.661C>G	NP_001186311.1:p.Gln221Glu
NM_144726.3:c.703C>G	NP_653327.1:p.Gln235Glu