Canonical Allele Identifier: CA2255461880

Gene: RNF135

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30997289C= , CM000679.2:g.30997289C=	GRCh38
NC_000017.10:g.29324307C= , CM000679.1:g.29324307C=	GRCh37
NC_000017.9:g.26348433C=	NCBI36
NG_011701.1:g.31352C=

Transcript Alleles

HGVS	Amino-acid Change
NM_032322.4:c.727C= MANE Select	NP_115698.3:p.Gln243=
ENST00000328381.10:c.727C= MANE Select	ENSP00000328340.5:p.Gln243=
NM_001184992.1:c.792C=	NP_001171921.1:p.Thr264=
NM_001184992.2:c.792C=	NP_001171921.1:p.Thr264=
NM_032322.3:c.727C=	NP_115698.3:p.Gln243=
NM_197939.1:c.564C=	NP_922921.1:p.Thr188=
NM_197939.2:c.564C=	NP_922921.1:p.Thr188=
ENST00000324689.8:c.564C=	ENSP00000323693.4:p.Thr188=
ENST00000328381.9:c.727C=	ENSP00000328340.5:p.Gln243=
ENST00000434242.2:c.143C=
ENST00000443677.6:c.420C=	ENSP00000411965.2:p.Thr140=
ENST00000535306.6:c.792C=	ENSP00000440470.2:p.Thr264=
XM_005258043.3:c.184C=	XP_005258100.1:p.Gln62=
XM_006722138.2:c.406C=	XP_006722201.1:p.Gln136=
XM_017025223.1:c.184C=	XP_016880712.1:p.Gln62=
XM_024451000.1:c.184C=	XP_024306768.1:p.Gln62=
XM_024451001.1:c.184C=	XP_024306769.1:p.Gln62=
XR_002958076.1:n.854C=
XR_002958077.1:n.789C=
XR_002958078.1:n.626C=