Canonical Allele Identifier: CA2255462386

Gene: RNF135

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998523G= , CM000679.2:g.30998523G=	GRCh38
NC_000017.10:g.29325541G= , CM000679.1:g.29325541G=	GRCh37
NC_000017.9:g.26349667G=	NCBI36
NG_011701.1:g.32586G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.770-139G= MANE Select	ENSP00000328340.5:n.770-139G=
ENST00000324689.8:c.607-139G=	ENSP00000323693.4:n.607-139G=
ENST00000328381.9:c.770-139G=	ENSP00000328340.5:n.770-139G=
ENST00000443677.6:c.463-139G=	ENSP00000411965.2:n.463-139G=
ENST00000535306.6:c.835-139G=	ENSP00000440470.2:n.835-139G=
NM_001184992.1:c.835-139G=	NP_001171921.1:n.835-139G=
NM_032322.3:c.770-139G=	NP_115698.3:n.770-139G=
NM_197939.1:c.607-139G=	NP_922921.1:n.607-139G=
XM_005258043.3:c.227-139G=	XP_005258100.1:n.227-139G=
XM_006722138.2:c.449-139G=	XP_006722201.1:n.449-139G=
XM_017025223.1:c.227-139G=	XP_016880712.1:n.227-139G=
XM_024451000.1:c.227-139G=	XP_024306768.1:n.227-139G=
XM_024451001.1:c.227-139G=	XP_024306769.1:n.227-139G=
XR_002958076.1:n.1103-139G=
XR_002958077.1:n.1038-139G=
XR_002958078.1:n.875-139G=
NM_032322.4:c.770-139G= MANE Select	NP_115698.3:n.770-139G=
NM_001184992.2:c.835-139G=	NP_001171921.1:n.835-139G=
NM_197939.2:c.607-139G=	NP_922921.1:n.607-139G=