Canonical Allele Identifier: CA447514149

Gene: RNF145

Linked Data

• MyVariant Identifiers: chr5:g.158603643A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159176635A>C , CM000667.2:g.159176635A>C	GRCh38
NC_000005.9:g.158603643A>C , CM000667.1:g.158603643A>C	GRCh37
NC_000005.8:g.158536221A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424310.7:c.618T>G MANE Select	ENSP00000409064.2:p.Val206=
ENST00000274542.6:c.702T>G	ENSP00000274542.2:p.Val234=
ENST00000424310.6:c.618T>G	ENSP00000409064.2:p.Val206=
ENST00000518802.5:c.708T>G	ENSP00000430955.1:p.Val236=
ENST00000519865.5:c.618T>G	ENSP00000430397.1:p.Val206=
ENST00000520638.1:c.660T>G	ENSP00000429071.1:p.Val220=
ENST00000521606.6:c.669T>G	ENSP00000430753.2:p.Val223=
ENST00000611185.4:c.618T>G	ENSP00000482720.1:p.Val206=
NM_001199380.1:c.708T>G	NP_001186309.1:p.Val236=
NM_001199381.1:c.669T>G	NP_001186310.1:p.Val223=
NM_001199382.1:c.660T>G	NP_001186311.1:p.Val220=
NM_001199383.1:c.618T>G	NP_001186312.1:p.Val206=
NM_144726.2:c.702T>G	NP_653327.1:p.Val234=
XM_005265826.3:c.666T>G	XP_005265883.1:p.Val222=
XM_017009138.2:c.618T>G	XP_016864627.1:p.Val206=
XM_024454383.1:c.666T>G	XP_024310151.1:p.Val222=
NM_001199381.2:c.669T>G	NP_001186310.1:p.Val223=
NM_001199383.2:c.618T>G MANE Select	NP_001186312.1:p.Val206=
NM_001199380.2:c.708T>G	NP_001186309.1:p.Val236=
NM_001199382.2:c.660T>G	NP_001186311.1:p.Val220=
NM_144726.3:c.702T>G	NP_653327.1:p.Val234=