Canonical Allele Identifier: CA399203103

Gene: RNF135

Linked Data

• MyVariant Identifiers: chr17:g.29325778T>G (hg19) ; chr17:g.30998760T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998760T>G , CM000679.2:g.30998760T>G	GRCh38
NC_000017.10:g.29325778T>G , CM000679.1:g.29325778T>G	GRCh37
NC_000017.9:g.26349904T>G	NCBI36
NG_011701.1:g.32823T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000328381.10:c.868T>G MANE Select	ENSP00000328340.5:p.Tyr290Asp
ENST00000324689.8:c.*72T>G	ENSP00000323693.4:n.*72T>G
ENST00000328381.9:c.868T>G	ENSP00000328340.5:p.Tyr290Asp
ENST00000443677.6:c.*72T>G	ENSP00000411965.2:n.*72T>G
ENST00000535306.6:c.*72T>G	ENSP00000440470.2:n.*72T>G
NM_001184992.1:c.*72T>G	NP_001171921.1:n.*72T>G
NM_032322.3:c.868T>G	NP_115698.3:p.Tyr290Asp
NM_197939.1:c.*72T>G	NP_922921.1:n.*72T>G
XM_005258043.3:c.325T>G	XP_005258100.1:p.Tyr109Asp
XM_006722138.2:c.547T>G	XP_006722201.1:p.Tyr183Asp
XM_017025223.1:c.325T>G	XP_016880712.1:p.Tyr109Asp
XM_024451000.1:c.325T>G	XP_024306768.1:p.Tyr109Asp
XM_024451001.1:c.325T>G	XP_024306769.1:p.Tyr109Asp
XR_002958077.1:n.1136T>G
NM_032322.4:c.868T>G MANE Select	NP_115698.3:p.Tyr290Asp
NM_001184992.2:c.*72T>G	NP_001171921.1:n.*72T>G
NM_197939.2:c.*72T>G	NP_922921.1:n.*72T>G