Canonical Allele Identifier: CA727985164

Gene: RNF135

Linked Data

• dbSNP Id: rs1369657848
• gnomAD v3: 17-30998391-AAAAT-A
• gnomAD v4: 17-30998391-AAAAT-A
• MyVariant Identifiers: chr17:g.29325410_29325413del (hg19) ; chr17:g.30998392_30998395del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998401_30998404del , CM000679.2:g.30998401_30998404del	GRCh38
NC_000017.10:g.29325419_29325422del , CM000679.1:g.29325419_29325422del	GRCh37
NC_000017.9:g.26349545_26349548del	NCBI36
NG_011701.1:g.32464_32467del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.770-261_770-258del MANE Select	ENSP00000328340.5:n.770-261_770-258del
ENST00000324689.8:c.607-261_607-258del	ENSP00000323693.4:n.607-261_607-258del
ENST00000328381.9:c.770-261_770-258del	ENSP00000328340.5:n.770-261_770-258del
ENST00000443677.6:c.463-261_463-258del	ENSP00000411965.2:n.463-261_463-258del
ENST00000535306.6:c.835-261_835-258del	ENSP00000440470.2:n.835-261_835-258del
NM_001184992.1:c.835-261_835-258del	NP_001171921.1:n.835-261_835-258del
NM_032322.3:c.770-261_770-258del	NP_115698.3:n.770-261_770-258del
NM_197939.1:c.607-261_607-258del	NP_922921.1:n.607-261_607-258del
XM_005258043.3:c.227-261_227-258del	XP_005258100.1:n.227-261_227-258del
XM_006722138.2:c.449-261_449-258del	XP_006722201.1:n.449-261_449-258del
XM_017025223.1:c.227-261_227-258del	XP_016880712.1:n.227-261_227-258del
XM_024451000.1:c.227-261_227-258del	XP_024306768.1:n.227-261_227-258del
XM_024451001.1:c.227-261_227-258del	XP_024306769.1:n.227-261_227-258del
XR_002958076.1:n.1103-261_1103-258del
XR_002958077.1:n.1038-261_1038-258del
XR_002958078.1:n.875-261_875-258del
NM_032322.4:c.770-261_770-258del MANE Select	NP_115698.3:n.770-261_770-258del
NM_001184992.2:c.835-261_835-258del	NP_001171921.1:n.835-261_835-258del
NM_197939.2:c.607-261_607-258del	NP_922921.1:n.607-261_607-258del