Canonical Allele Identifier: CA399202914

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325691C>A (hg19) ; chr17:g.30998673C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998673C>A , CM000679.2:g.30998673C>A	GRCh38
NC_000017.10:g.29325691C>A , CM000679.1:g.29325691C>A	GRCh37
NC_000017.9:g.26349817C>A	NCBI36
NG_011701.1:g.32736C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.781C>A MANE Select	ENSP00000328340.5:p.Pro261Thr
ENST00000324689.8:c.618C>A	ENSP00000323693.4:p.Ile206=
ENST00000328381.9:c.781C>A	ENSP00000328340.5:p.Pro261Thr
ENST00000443677.6:c.474C>A	ENSP00000411965.2:p.Ile158=
ENST00000535306.6:c.846C>A	ENSP00000440470.2:p.Ile282=
NM_001184992.1:c.846C>A	NP_001171921.1:p.Ile282=
NM_032322.3:c.781C>A	NP_115698.3:p.Pro261Thr
NM_197939.1:c.618C>A	NP_922921.1:p.Ile206=
XM_005258043.3:c.238C>A	XP_005258100.1:p.Pro80Thr
XM_006722138.2:c.460C>A	XP_006722201.1:p.Pro154Thr
XM_017025223.1:c.238C>A	XP_016880712.1:p.Pro80Thr
XM_024451000.1:c.238C>A	XP_024306768.1:p.Pro80Thr
XM_024451001.1:c.238C>A	XP_024306769.1:p.Pro80Thr
XR_002958076.1:n.1114C>A
XR_002958077.1:n.1049C>A
XR_002958078.1:n.886C>A
NM_032322.4:c.781C>A MANE Select	NP_115698.3:p.Pro261Thr
NM_001184992.2:c.846C>A	NP_001171921.1:p.Ile282=
NM_197939.2:c.618C>A	NP_922921.1:p.Ile206=