Canonical Allele Identifier: CA399202943

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325701A>T (hg19) ; chr17:g.30998683A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998683A>T , CM000679.2:g.30998683A>T	GRCh38
NC_000017.10:g.29325701A>T , CM000679.1:g.29325701A>T	GRCh37
NC_000017.9:g.26349827A>T	NCBI36
NG_011701.1:g.32746A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.791A>T MANE Select	ENSP00000328340.5:p.Asn264Ile
ENST00000324689.8:c.628A>T	ENSP00000323693.4:p.Thr210Ser
ENST00000328381.9:c.791A>T	ENSP00000328340.5:p.Asn264Ile
ENST00000443677.6:c.484A>T	ENSP00000411965.2:p.Thr162Ser
ENST00000535306.6:c.856A>T	ENSP00000440470.2:p.Thr286Ser
NM_001184992.1:c.856A>T	NP_001171921.1:p.Thr286Ser
NM_032322.3:c.791A>T	NP_115698.3:p.Asn264Ile
NM_197939.1:c.628A>T	NP_922921.1:p.Thr210Ser
XM_005258043.3:c.248A>T	XP_005258100.1:p.Asn83Ile
XM_006722138.2:c.470A>T	XP_006722201.1:p.Asn157Ile
XM_017025223.1:c.248A>T	XP_016880712.1:p.Asn83Ile
XM_024451000.1:c.248A>T	XP_024306768.1:p.Asn83Ile
XM_024451001.1:c.248A>T	XP_024306769.1:p.Asn83Ile
XR_002958076.1:n.1124A>T
XR_002958077.1:n.1059A>T
XR_002958078.1:n.896A>T
NM_032322.4:c.791A>T MANE Select	NP_115698.3:p.Asn264Ile
NM_001184992.2:c.856A>T	NP_001171921.1:p.Thr286Ser
NM_197939.2:c.628A>T	NP_922921.1:p.Thr210Ser