Canonical Allele Identifier: CA727985168

Gene: RNF135

Linked Data

• dbSNP Id: rs1460756899
• gnomAD v3: 17-30998400-AAATAT-A
• gnomAD v4: 17-30998400-AAATAT-A
• MyVariant Identifiers: chr17:g.29325419_29325423del (hg19) ; chr17:g.30998401_30998405del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998405_30998409del , CM000679.2:g.30998405_30998409del	GRCh38
NC_000017.10:g.29325423_29325427del , CM000679.1:g.29325423_29325427del	GRCh37
NC_000017.9:g.26349549_26349553del	NCBI36
NG_011701.1:g.32468_32472del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.770-257_770-253del MANE Select	ENSP00000328340.5:n.770-257_770-253del
ENST00000324689.8:c.607-257_607-253del	ENSP00000323693.4:n.607-257_607-253del
ENST00000328381.9:c.770-257_770-253del	ENSP00000328340.5:n.770-257_770-253del
ENST00000443677.6:c.463-257_463-253del	ENSP00000411965.2:n.463-257_463-253del
ENST00000535306.6:c.835-257_835-253del	ENSP00000440470.2:n.835-257_835-253del
NM_001184992.1:c.835-257_835-253del	NP_001171921.1:n.835-257_835-253del
NM_032322.3:c.770-257_770-253del	NP_115698.3:n.770-257_770-253del
NM_197939.1:c.607-257_607-253del	NP_922921.1:n.607-257_607-253del
XM_005258043.3:c.227-257_227-253del	XP_005258100.1:n.227-257_227-253del
XM_006722138.2:c.449-257_449-253del	XP_006722201.1:n.449-257_449-253del
XM_017025223.1:c.227-257_227-253del	XP_016880712.1:n.227-257_227-253del
XM_024451000.1:c.227-257_227-253del	XP_024306768.1:n.227-257_227-253del
XM_024451001.1:c.227-257_227-253del	XP_024306769.1:n.227-257_227-253del
XR_002958076.1:n.1103-257_1103-253del
XR_002958077.1:n.1038-257_1038-253del
XR_002958078.1:n.875-257_875-253del
NM_032322.4:c.770-257_770-253del MANE Select	NP_115698.3:n.770-257_770-253del
NM_001184992.2:c.835-257_835-253del	NP_001171921.1:n.835-257_835-253del
NM_197939.2:c.607-257_607-253del	NP_922921.1:n.607-257_607-253del