Canonical Allele Identifier: CA399202899

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325686T>A (hg19) ; chr17:g.30998668T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998668T>A , CM000679.2:g.30998668T>A	GRCh38
NC_000017.10:g.29325686T>A , CM000679.1:g.29325686T>A	GRCh37
NC_000017.9:g.26349812T>A	NCBI36
NG_011701.1:g.32731T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.776T>A MANE Select	ENSP00000328340.5:p.Ile259Asn
ENST00000324689.8:c.613T>A	ENSP00000323693.4:p.Ser205Thr
ENST00000328381.9:c.776T>A	ENSP00000328340.5:p.Ile259Asn
ENST00000443677.6:c.469T>A	ENSP00000411965.2:p.Ser157Thr
ENST00000535306.6:c.841T>A	ENSP00000440470.2:p.Ser281Thr
NM_001184992.1:c.841T>A	NP_001171921.1:p.Ser281Thr
NM_032322.3:c.776T>A	NP_115698.3:p.Ile259Asn
NM_197939.1:c.613T>A	NP_922921.1:p.Ser205Thr
XM_005258043.3:c.233T>A	XP_005258100.1:p.Ile78Asn
XM_006722138.2:c.455T>A	XP_006722201.1:p.Ile152Asn
XM_017025223.1:c.233T>A	XP_016880712.1:p.Ile78Asn
XM_024451000.1:c.233T>A	XP_024306768.1:p.Ile78Asn
XM_024451001.1:c.233T>A	XP_024306769.1:p.Ile78Asn
XR_002958076.1:n.1109T>A
XR_002958077.1:n.1044T>A
XR_002958078.1:n.881T>A
NM_032322.4:c.776T>A MANE Select	NP_115698.3:p.Ile259Asn
NM_001184992.2:c.841T>A	NP_001171921.1:p.Ser281Thr
NM_197939.2:c.613T>A	NP_922921.1:p.Ser205Thr