Canonical Allele Identifier: CA361901134

Gene: RNF145

Linked Data

• gnomAD v4: 5-159176634-G-T
• MyVariant Identifiers: chr5:g.158603642G>T (hg19) ; chr5:g.159176634G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424310.7:c.619C>A MANE Select	ENSP00000409064.2:p.Gln207Lys
ENST00000274542.6:c.703C>A	ENSP00000274542.2:p.Gln235Lys
ENST00000424310.6:c.619C>A	ENSP00000409064.2:p.Gln207Lys
ENST00000518802.5:c.709C>A	ENSP00000430955.1:p.Gln237Lys
ENST00000519865.5:c.619C>A	ENSP00000430397.1:p.Gln207Lys
ENST00000520638.1:c.661C>A	ENSP00000429071.1:p.Gln221Lys
ENST00000521606.6:c.670C>A	ENSP00000430753.2:p.Gln224Lys
ENST00000611185.4:c.619C>A	ENSP00000482720.1:p.Gln207Lys
NM_001199380.1:c.709C>A	NP_001186309.1:p.Gln237Lys
NM_001199381.1:c.670C>A	NP_001186310.1:p.Gln224Lys
NM_001199382.1:c.661C>A	NP_001186311.1:p.Gln221Lys
NM_001199383.1:c.619C>A	NP_001186312.1:p.Gln207Lys
NM_144726.2:c.703C>A	NP_653327.1:p.Gln235Lys
XM_005265826.3:c.667C>A	XP_005265883.1:p.Gln223Lys
XM_017009138.2:c.619C>A	XP_016864627.1:p.Gln207Lys
XM_024454383.1:c.667C>A	XP_024310151.1:p.Gln223Lys
NM_001199381.2:c.670C>A	NP_001186310.1:p.Gln224Lys
NM_001199383.2:c.619C>A MANE Select	NP_001186312.1:p.Gln207Lys
NM_001199380.2:c.709C>A	NP_001186309.1:p.Gln237Lys
NM_001199382.2:c.661C>A	NP_001186311.1:p.Gln221Lys
NM_144726.3:c.703C>A	NP_653327.1:p.Gln235Lys