Canonical Allele Identifier: CA2255443592

Gene: RNF135

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998804T= , CM000679.2:g.30998804T=	GRCh38
NC_000017.10:g.29325822T= , CM000679.1:g.29325822T=	GRCh37
NC_000017.9:g.26349948T=	NCBI36
NG_011701.1:g.32867T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.912T= MANE Select	ENSP00000328340.5:p.Cys304=
ENST00000324689.8:c.*116T=	ENSP00000323693.4:n.*116T=
ENST00000328381.9:c.912T=	ENSP00000328340.5:p.Cys304=
ENST00000443677.6:c.*116T=	ENSP00000411965.2:n.*116T=
ENST00000535306.6:c.*116T=	ENSP00000440470.2:n.*116T=
NM_001184992.1:c.*116T=	NP_001171921.1:n.*116T=
NM_032322.3:c.912T=	NP_115698.3:p.Cys304=
NM_197939.1:c.*116T=	NP_922921.1:n.*116T=
XM_005258043.3:c.369T=	XP_005258100.1:p.Cys123=
XM_006722138.2:c.591T=	XP_006722201.1:p.Cys197=
XM_017025223.1:c.369T=	XP_016880712.1:p.Cys123=
XM_024451000.1:c.369T=	XP_024306768.1:p.Cys123=
XM_024451001.1:c.369T=	XP_024306769.1:p.Cys123=
XR_002958077.1:n.1180T=
NM_032322.4:c.912T= MANE Select	NP_115698.3:p.Cys304=
NM_001184992.2:c.*116T=	NP_001171921.1:n.*116T=
NM_197939.2:c.*116T=	NP_922921.1:n.*116T=