Canonical Allele Identifier: CA8485331

Gene: RNF135

Linked Data

• dbSNP Id: rs769263188
• ExAC: 17:29325675 C / CA
• MyVariant Identifiers: chr17:g.29325675_29325676insA (hg19) ; chr17:g.30998657_30998658insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998660dup , CM000679.2:g.30998660dup	GRCh38
NC_000017.10:g.29325678dup , CM000679.1:g.29325678dup	GRCh37
NC_000017.9:g.26349804dup	NCBI36
NG_011701.1:g.32723dup

Transcript Alleles

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