Canonical Allele Identifier: CA399202932

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325697T>G (hg19) ; chr17:g.30998679T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998679T>G , CM000679.2:g.30998679T>G	GRCh38
NC_000017.10:g.29325697T>G , CM000679.1:g.29325697T>G	GRCh37
NC_000017.9:g.26349823T>G	NCBI36
NG_011701.1:g.32742T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.787T>G MANE Select	ENSP00000328340.5:p.Phe263Val
ENST00000324689.8:c.624T>G	ENSP00000323693.4:p.Pro208=
ENST00000328381.9:c.787T>G	ENSP00000328340.5:p.Phe263Val
ENST00000443677.6:c.480T>G	ENSP00000411965.2:p.Pro160=
ENST00000535306.6:c.852T>G	ENSP00000440470.2:p.Pro284=
NM_001184992.1:c.852T>G	NP_001171921.1:p.Pro284=
NM_032322.3:c.787T>G	NP_115698.3:p.Phe263Val
NM_197939.1:c.624T>G	NP_922921.1:p.Pro208=
XM_005258043.3:c.244T>G	XP_005258100.1:p.Phe82Val
XM_006722138.2:c.466T>G	XP_006722201.1:p.Phe156Val
XM_017025223.1:c.244T>G	XP_016880712.1:p.Phe82Val
XM_024451000.1:c.244T>G	XP_024306768.1:p.Phe82Val
XM_024451001.1:c.244T>G	XP_024306769.1:p.Phe82Val
XR_002958076.1:n.1120T>G
XR_002958077.1:n.1055T>G
XR_002958078.1:n.892T>G
NM_032322.4:c.787T>G MANE Select	NP_115698.3:p.Phe263Val
NM_001184992.2:c.852T>G	NP_001171921.1:p.Pro284=
NM_197939.2:c.624T>G	NP_922921.1:p.Pro208=