Canonical Allele Identifier: CA399202885

Gene: RNF135

Linked Data

• dbSNP Id: rs1412363653
• gnomAD v2: 17-29325681-G-A
• gnomAD v3: 17-30998663-G-A
• gnomAD v4: 17-30998663-G-A
• MyVariant Identifiers: chr17:g.29325681G>A (hg19) ; chr17:g.30998663G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998663G>A , CM000679.2:g.30998663G>A	GRCh38
NC_000017.10:g.29325681G>A , CM000679.1:g.29325681G>A	GRCh37
NC_000017.9:g.26349807G>A	NCBI36
NG_011701.1:g.32726G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.771G>A MANE Select	ENSP00000328340.5:p.Trp257Ter
ENST00000324689.8:c.608G>A	ENSP00000323693.4:p.Gly203Glu
ENST00000328381.9:c.771G>A	ENSP00000328340.5:p.Trp257Ter
ENST00000443677.6:c.464G>A	ENSP00000411965.2:p.Gly155Glu
ENST00000535306.6:c.836G>A	ENSP00000440470.2:p.Gly279Glu
NM_001184992.1:c.836G>A	NP_001171921.1:p.Gly279Glu
NM_032322.3:c.771G>A	NP_115698.3:p.Trp257Ter
NM_197939.1:c.608G>A	NP_922921.1:p.Gly203Glu
XM_005258043.3:c.228G>A	XP_005258100.1:p.Trp76Ter
XM_006722138.2:c.450G>A	XP_006722201.1:p.Trp150Ter
XM_017025223.1:c.228G>A	XP_016880712.1:p.Trp76Ter
XM_024451000.1:c.228G>A	XP_024306768.1:p.Trp76Ter
XM_024451001.1:c.228G>A	XP_024306769.1:p.Trp76Ter
XR_002958076.1:n.1104G>A
XR_002958077.1:n.1039G>A
XR_002958078.1:n.876G>A
NM_032322.4:c.771G>A MANE Select	NP_115698.3:p.Trp257Ter
NM_001184992.2:c.836G>A	NP_001171921.1:p.Gly279Glu
NM_197939.2:c.608G>A	NP_922921.1:p.Gly203Glu