Canonical Allele Identifier: CA447514140

Gene: RNF145

Linked Data

• MyVariant Identifiers: chr5:g.158603640C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159176632C>T , CM000667.2:g.159176632C>T	GRCh38
NC_000005.9:g.158603640C>T , CM000667.1:g.158603640C>T	GRCh37
NC_000005.8:g.158536218C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424310.7:c.621G>A MANE Select	ENSP00000409064.2:p.Gln207=
ENST00000274542.6:c.705G>A	ENSP00000274542.2:p.Gln235=
ENST00000424310.6:c.621G>A	ENSP00000409064.2:p.Gln207=
ENST00000518802.5:c.711G>A	ENSP00000430955.1:p.Gln237=
ENST00000519865.5:c.621G>A	ENSP00000430397.1:p.Gln207=
ENST00000520638.1:c.663G>A	ENSP00000429071.1:p.Gln221=
ENST00000521606.6:c.672G>A	ENSP00000430753.2:p.Gln224=
ENST00000611185.4:c.621G>A	ENSP00000482720.1:p.Gln207=
NM_001199380.1:c.711G>A	NP_001186309.1:p.Gln237=
NM_001199381.1:c.672G>A	NP_001186310.1:p.Gln224=
NM_001199382.1:c.663G>A	NP_001186311.1:p.Gln221=
NM_001199383.1:c.621G>A	NP_001186312.1:p.Gln207=
NM_144726.2:c.705G>A	NP_653327.1:p.Gln235=
XM_005265826.3:c.669G>A	XP_005265883.1:p.Gln223=
XM_017009138.2:c.621G>A	XP_016864627.1:p.Gln207=
XM_024454383.1:c.669G>A	XP_024310151.1:p.Gln223=
NM_001199381.2:c.672G>A	NP_001186310.1:p.Gln224=
NM_001199383.2:c.621G>A MANE Select	NP_001186312.1:p.Gln207=
NM_001199380.2:c.711G>A	NP_001186309.1:p.Gln237=
NM_001199382.2:c.663G>A	NP_001186311.1:p.Gln221=
NM_144726.3:c.705G>A	NP_653327.1:p.Gln235=