Canonical Allele Identifier: CA399202891

Gene: RNF135

Linked Data

• gnomAD v4: 17-30998665-C-T
• MyVariant Identifiers: chr17:g.29325683C>T (hg19) ; chr17:g.30998665C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998665C>T , CM000679.2:g.30998665C>T	GRCh38
NC_000017.10:g.29325683C>T , CM000679.1:g.29325683C>T	GRCh37
NC_000017.9:g.26349809C>T	NCBI36
NG_011701.1:g.32728C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.773C>T MANE Select	ENSP00000328340.5:p.Ala258Val
ENST00000324689.8:c.610C>T	ENSP00000323693.4:p.Pro204Ser
ENST00000328381.9:c.773C>T	ENSP00000328340.5:p.Ala258Val
ENST00000443677.6:c.466C>T	ENSP00000411965.2:p.Pro156Ser
ENST00000535306.6:c.838C>T	ENSP00000440470.2:p.Pro280Ser
NM_001184992.1:c.838C>T	NP_001171921.1:p.Pro280Ser
NM_032322.3:c.773C>T	NP_115698.3:p.Ala258Val
NM_197939.1:c.610C>T	NP_922921.1:p.Pro204Ser
XM_005258043.3:c.230C>T	XP_005258100.1:p.Ala77Val
XM_006722138.2:c.452C>T	XP_006722201.1:p.Ala151Val
XM_017025223.1:c.230C>T	XP_016880712.1:p.Ala77Val
XM_024451000.1:c.230C>T	XP_024306768.1:p.Ala77Val
XM_024451001.1:c.230C>T	XP_024306769.1:p.Ala77Val
XR_002958076.1:n.1106C>T
XR_002958077.1:n.1041C>T
XR_002958078.1:n.878C>T
NM_032322.4:c.773C>T MANE Select	NP_115698.3:p.Ala258Val
NM_001184992.2:c.838C>T	NP_001171921.1:p.Pro280Ser
NM_197939.2:c.610C>T	NP_922921.1:p.Pro204Ser