Canonical Allele Identifier: CA2255462457

Gene: RNF135

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998663G= , CM000679.2:g.30998663G=	GRCh38
NC_000017.10:g.29325681G= , CM000679.1:g.29325681G=	GRCh37
NC_000017.9:g.26349807G=	NCBI36
NG_011701.1:g.32726G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.771G= MANE Select	ENSP00000328340.5:p.Trp257=
ENST00000324689.8:c.608G=	ENSP00000323693.4:p.Gly203=
ENST00000328381.9:c.771G=	ENSP00000328340.5:p.Trp257=
ENST00000443677.6:c.464G=	ENSP00000411965.2:p.Gly155=
ENST00000535306.6:c.836G=	ENSP00000440470.2:p.Gly279=
NM_001184992.1:c.836G=	NP_001171921.1:p.Gly279=
NM_032322.3:c.771G=	NP_115698.3:p.Trp257=
NM_197939.1:c.608G=	NP_922921.1:p.Gly203=
XM_005258043.3:c.228G=	XP_005258100.1:p.Trp76=
XM_006722138.2:c.450G=	XP_006722201.1:p.Trp150=
XM_017025223.1:c.228G=	XP_016880712.1:p.Trp76=
XM_024451000.1:c.228G=	XP_024306768.1:p.Trp76=
XM_024451001.1:c.228G=	XP_024306769.1:p.Trp76=
XR_002958076.1:n.1104G=
XR_002958077.1:n.1039G=
XR_002958078.1:n.876G=
NM_032322.4:c.771G= MANE Select	NP_115698.3:p.Trp257=
NM_001184992.2:c.836G=	NP_001171921.1:p.Gly279=
NM_197939.2:c.608G=	NP_922921.1:p.Gly203=