Canonical Allele Identifier: CA399203117

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325785G>T (hg19) ; chr17:g.30998767G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998767G>T , CM000679.2:g.30998767G>T	GRCh38
NC_000017.10:g.29325785G>T , CM000679.1:g.29325785G>T	GRCh37
NC_000017.9:g.26349911G>T	NCBI36
NG_011701.1:g.32830G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.875G>T MANE Select	ENSP00000328340.5:p.Trp292Leu
ENST00000324689.8:c.*79G>T	ENSP00000323693.4:n.*79G>T
ENST00000328381.9:c.875G>T	ENSP00000328340.5:p.Trp292Leu
ENST00000443677.6:c.*79G>T	ENSP00000411965.2:n.*79G>T
ENST00000535306.6:c.*79G>T	ENSP00000440470.2:n.*79G>T
NM_001184992.1:c.*79G>T	NP_001171921.1:n.*79G>T
NM_032322.3:c.875G>T	NP_115698.3:p.Trp292Leu
NM_197939.1:c.*79G>T	NP_922921.1:n.*79G>T
XM_005258043.3:c.332G>T	XP_005258100.1:p.Trp111Leu
XM_006722138.2:c.554G>T	XP_006722201.1:p.Trp185Leu
XM_017025223.1:c.332G>T	XP_016880712.1:p.Trp111Leu
XM_024451000.1:c.332G>T	XP_024306768.1:p.Trp111Leu
XM_024451001.1:c.332G>T	XP_024306769.1:p.Trp111Leu
XR_002958077.1:n.1143G>T
NM_032322.4:c.875G>T MANE Select	NP_115698.3:p.Trp292Leu
NM_001184992.2:c.*79G>T	NP_001171921.1:n.*79G>T
NM_197939.2:c.*79G>T	NP_922921.1:n.*79G>T