Canonical Allele Identifier: CA2255443614

Gene: RNF135

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998822T= , CM000679.2:g.30998822T=	GRCh38
NC_000017.10:g.29325840T= , CM000679.1:g.29325840T=	GRCh37
NC_000017.9:g.26349966T=	NCBI36
NG_011701.1:g.32885T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.930T= MANE Select	ENSP00000328340.5:p.Ser310=
ENST00000324689.8:c.*134T=	ENSP00000323693.4:n.*134T=
ENST00000328381.9:c.930T=	ENSP00000328340.5:p.Ser310=
ENST00000443677.6:c.*134T=	ENSP00000411965.2:n.*134T=
ENST00000535306.6:c.*134T=	ENSP00000440470.2:n.*134T=
NM_001184992.1:c.*134T=	NP_001171921.1:n.*134T=
NM_032322.3:c.930T=	NP_115698.3:p.Ser310=
NM_197939.1:c.*134T=	NP_922921.1:n.*134T=
XM_005258043.3:c.387T=	XP_005258100.1:p.Ser129=
XM_006722138.2:c.609T=	XP_006722201.1:p.Ser203=
XM_017025223.1:c.387T=	XP_016880712.1:p.Ser129=
XM_024451000.1:c.387T=	XP_024306768.1:p.Ser129=
XM_024451001.1:c.387T=	XP_024306769.1:p.Ser129=
XR_002958077.1:n.1198T=
NM_032322.4:c.930T= MANE Select	NP_115698.3:p.Ser310=
NM_001184992.2:c.*134T=	NP_001171921.1:n.*134T=
NM_197939.2:c.*134T=	NP_922921.1:n.*134T=