Canonical Allele Identifier: CA399202908

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325689A>G (hg19) ; chr17:g.30998671A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998671A>G , CM000679.2:g.30998671A>G	GRCh38
NC_000017.10:g.29325689A>G , CM000679.1:g.29325689A>G	GRCh37
NC_000017.9:g.26349815A>G	NCBI36
NG_011701.1:g.32734A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.779A>G MANE Select	ENSP00000328340.5:p.His260Arg
ENST00000324689.8:c.616A>G	ENSP00000323693.4:p.Ile206Val
ENST00000328381.9:c.779A>G	ENSP00000328340.5:p.His260Arg
ENST00000443677.6:c.472A>G	ENSP00000411965.2:p.Ile158Val
ENST00000535306.6:c.844A>G	ENSP00000440470.2:p.Ile282Val
NM_001184992.1:c.844A>G	NP_001171921.1:p.Ile282Val
NM_032322.3:c.779A>G	NP_115698.3:p.His260Arg
NM_197939.1:c.616A>G	NP_922921.1:p.Ile206Val
XM_005258043.3:c.236A>G	XP_005258100.1:p.His79Arg
XM_006722138.2:c.458A>G	XP_006722201.1:p.His153Arg
XM_017025223.1:c.236A>G	XP_016880712.1:p.His79Arg
XM_024451000.1:c.236A>G	XP_024306768.1:p.His79Arg
XM_024451001.1:c.236A>G	XP_024306769.1:p.His79Arg
XR_002958076.1:n.1112A>G
XR_002958077.1:n.1047A>G
XR_002958078.1:n.884A>G
NM_032322.4:c.779A>G MANE Select	NP_115698.3:p.His260Arg
NM_001184992.2:c.844A>G	NP_001171921.1:p.Ile282Val
NM_197939.2:c.616A>G	NP_922921.1:p.Ile206Val