Canonical Allele Identifier: CA2255462489

Gene: RNF135

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998737_30998739delinsCTG , CM000679.2:g.30998737_30998739delinsCTG	GRCh38
NC_000017.10:g.29325755_29325757delinsCTG , CM000679.1:g.29325755_29325757delinsCTG	GRCh37
NC_000017.9:g.26349881_26349883delinsCTG	NCBI36
NG_011701.1:g.32800_32802delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.845_847delinsCTG MANE Select	ENSP00000328340.5:p.Thr282=
ENST00000324689.8:c.*49_*51delinsCTG	ENSP00000323693.4:n.*49_*51delinsCTG
ENST00000328381.9:c.845_847delinsCTG	ENSP00000328340.5:p.Thr282=
ENST00000443677.6:c.*49_*51delinsCTG	ENSP00000411965.2:n.*49_*51delinsCTG
ENST00000535306.6:c.*49_*51delinsCTG	ENSP00000440470.2:n.*49_*51delinsCTG
NM_001184992.1:c.*49_*51delinsCTG	NP_001171921.1:n.*49_*51delinsCTG
NM_032322.3:c.845_847delinsCTG	NP_115698.3:p.Thr282=
NM_197939.1:c.*49_*51delinsCTG	NP_922921.1:n.*49_*51delinsCTG
XM_005258043.3:c.302_304delinsCTG	XP_005258100.1:p.Thr101=
XM_006722138.2:c.524_526delinsCTG	XP_006722201.1:p.Thr175=
XM_017025223.1:c.302_304delinsCTG	XP_016880712.1:p.Thr101=
XM_024451000.1:c.302_304delinsCTG	XP_024306768.1:p.Thr101=
XM_024451001.1:c.302_304delinsCTG	XP_024306769.1:p.Thr101=
XR_002958076.1:n.1178_1180delinsCTG
XR_002958077.1:n.1113_1115delinsCTG
XR_002958078.1:n.950_952delinsCTG
NM_032322.4:c.845_847delinsCTG MANE Select	NP_115698.3:p.Thr282=
NM_001184992.2:c.*49_*51delinsCTG	NP_001171921.1:n.*49_*51delinsCTG
NM_197939.2:c.*49_*51delinsCTG	NP_922921.1:n.*49_*51delinsCTG