Canonical Allele Identifier: CA8485326

Gene: RNF135

Linked Data

• dbSNP Id: rs111718437
• ExAC: 17:29325662 CT / C
• gnomAD v2: 17-29325662-CT-C
• gnomAD v3: 17-30998644-CT-C
• gnomAD v4: 17-30998644-CT-C
• MyVariant Identifiers: chr17:g.29325664del (hg19) ; chr17:g.29325663del (hg19) ; chr17:g.30998645del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998655del , CM000679.2:g.30998655del	GRCh38
NC_000017.10:g.29325673del , CM000679.1:g.29325673del	GRCh37
NC_000017.9:g.26349799del	NCBI36
NG_011701.1:g.32718del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.770-7del MANE Select	ENSP00000328340.5:n.770-7del
ENST00000324689.8:c.607-7del	ENSP00000323693.4:n.607-7del
ENST00000328381.9:c.770-7del	ENSP00000328340.5:n.770-7del
ENST00000443677.6:c.463-7del	ENSP00000411965.2:n.463-7del
ENST00000535306.6:c.835-7del	ENSP00000440470.2:n.835-7del
NM_001184992.1:c.835-7del	NP_001171921.1:n.835-7del
NM_032322.3:c.770-7del	NP_115698.3:n.770-7del
NM_197939.1:c.607-7del	NP_922921.1:n.607-7del
XM_005258043.3:c.227-7del	XP_005258100.1:n.227-7del
XM_006722138.2:c.449-7del	XP_006722201.1:n.449-7del
XM_017025223.1:c.227-7del	XP_016880712.1:n.227-7del
XM_024451000.1:c.227-7del	XP_024306768.1:n.227-7del
XM_024451001.1:c.227-7del	XP_024306769.1:n.227-7del
XR_002958076.1:n.1103-7del
XR_002958077.1:n.1038-7del
XR_002958078.1:n.875-7del
NM_032322.4:c.770-7del MANE Select	NP_115698.3:n.770-7del
NM_001184992.2:c.835-7del	NP_001171921.1:n.835-7del
NM_197939.2:c.607-7del	NP_922921.1:n.607-7del