Canonical Allele Identifier: CA361901127

Gene: RNF145

Linked Data

• MyVariant Identifiers: chr5:g.158603641T>G (hg19) ; chr5:g.159176633T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159176633T>G , CM000667.2:g.159176633T>G	GRCh38
NC_000005.9:g.158603641T>G , CM000667.1:g.158603641T>G	GRCh37
NC_000005.8:g.158536219T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424310.7:c.620A>C MANE Select	ENSP00000409064.2:p.Gln207Pro
ENST00000274542.6:c.704A>C	ENSP00000274542.2:p.Gln235Pro
ENST00000424310.6:c.620A>C	ENSP00000409064.2:p.Gln207Pro
ENST00000518802.5:c.710A>C	ENSP00000430955.1:p.Gln237Pro
ENST00000519865.5:c.620A>C	ENSP00000430397.1:p.Gln207Pro
ENST00000520638.1:c.662A>C	ENSP00000429071.1:p.Gln221Pro
ENST00000521606.6:c.671A>C	ENSP00000430753.2:p.Gln224Pro
ENST00000611185.4:c.620A>C	ENSP00000482720.1:p.Gln207Pro
NM_001199380.1:c.710A>C	NP_001186309.1:p.Gln237Pro
NM_001199381.1:c.671A>C	NP_001186310.1:p.Gln224Pro
NM_001199382.1:c.662A>C	NP_001186311.1:p.Gln221Pro
NM_001199383.1:c.620A>C	NP_001186312.1:p.Gln207Pro
NM_144726.2:c.704A>C	NP_653327.1:p.Gln235Pro
XM_005265826.3:c.668A>C	XP_005265883.1:p.Gln223Pro
XM_017009138.2:c.620A>C	XP_016864627.1:p.Gln207Pro
XM_024454383.1:c.668A>C	XP_024310151.1:p.Gln223Pro
NM_001199381.2:c.671A>C	NP_001186310.1:p.Gln224Pro
NM_001199383.2:c.620A>C MANE Select	NP_001186312.1:p.Gln207Pro
NM_001199380.2:c.710A>C	NP_001186309.1:p.Gln237Pro
NM_001199382.2:c.662A>C	NP_001186311.1:p.Gln221Pro
NM_144726.3:c.704A>C	NP_653327.1:p.Gln235Pro