Canonical Allele Identifier: CA2255462458

Gene: RNF135

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998667A= , CM000679.2:g.30998667A=	GRCh38
NC_000017.10:g.29325685A= , CM000679.1:g.29325685A=	GRCh37
NC_000017.9:g.26349811A=	NCBI36
NG_011701.1:g.32730A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.775A= MANE Select	ENSP00000328340.5:p.Ile259=
ENST00000324689.8:c.612A=	ENSP00000323693.4:p.Pro204=
ENST00000328381.9:c.775A=	ENSP00000328340.5:p.Ile259=
ENST00000443677.6:c.468A=	ENSP00000411965.2:p.Pro156=
ENST00000535306.6:c.840A=	ENSP00000440470.2:p.Pro280=
NM_001184992.1:c.840A=	NP_001171921.1:p.Pro280=
NM_032322.3:c.775A=	NP_115698.3:p.Ile259=
NM_197939.1:c.612A=	NP_922921.1:p.Pro204=
XM_005258043.3:c.232A=	XP_005258100.1:p.Ile78=
XM_006722138.2:c.454A=	XP_006722201.1:p.Ile152=
XM_017025223.1:c.232A=	XP_016880712.1:p.Ile78=
XM_024451000.1:c.232A=	XP_024306768.1:p.Ile78=
XM_024451001.1:c.232A=	XP_024306769.1:p.Ile78=
XR_002958076.1:n.1108A=
XR_002958077.1:n.1043A=
XR_002958078.1:n.880A=
NM_032322.4:c.775A= MANE Select	NP_115698.3:p.Ile259=
NM_001184992.2:c.840A=	NP_001171921.1:p.Pro280=
NM_197939.2:c.612A=	NP_922921.1:p.Pro204=