Canonical Allele Identifier: CA2255462348

Gene: RNF135

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998400_30998405delinsAAATAT , CM000679.2:g.30998400_30998405delinsAAATAT	GRCh38
NC_000017.10:g.29325418_29325423delinsAAATAT , CM000679.1:g.29325418_29325423delinsAAATAT	GRCh37
NC_000017.9:g.26349544_26349549delinsAAATAT	NCBI36
NG_011701.1:g.32463_32468delinsAAATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.770-262_770-257delinsAAATAT MANE Select	ENSP00000328340.5:n.770-262_770-257delinsAAATAT
ENST00000324689.8:c.607-262_607-257delinsAAATAT	ENSP00000323693.4:n.607-262_607-257delinsAAATAT
ENST00000328381.9:c.770-262_770-257delinsAAATAT	ENSP00000328340.5:n.770-262_770-257delinsAAATAT
ENST00000443677.6:c.463-262_463-257delinsAAATAT	ENSP00000411965.2:n.463-262_463-257delinsAAATAT
ENST00000535306.6:c.835-262_835-257delinsAAATAT	ENSP00000440470.2:n.835-262_835-257delinsAAATAT
NM_001184992.1:c.835-262_835-257delinsAAATAT	NP_001171921.1:n.835-262_835-257delinsAAATAT
NM_032322.3:c.770-262_770-257delinsAAATAT	NP_115698.3:n.770-262_770-257delinsAAATAT
NM_197939.1:c.607-262_607-257delinsAAATAT	NP_922921.1:n.607-262_607-257delinsAAATAT
XM_005258043.3:c.227-262_227-257delinsAAATAT	XP_005258100.1:n.227-262_227-257delinsAAATAT
XM_006722138.2:c.449-262_449-257delinsAAATAT	XP_006722201.1:n.449-262_449-257delinsAAATAT
XM_017025223.1:c.227-262_227-257delinsAAATAT	XP_016880712.1:n.227-262_227-257delinsAAATAT
XM_024451000.1:c.227-262_227-257delinsAAATAT	XP_024306768.1:n.227-262_227-257delinsAAATAT
XM_024451001.1:c.227-262_227-257delinsAAATAT	XP_024306769.1:n.227-262_227-257delinsAAATAT
XR_002958076.1:n.1103-262_1103-257delinsAAATAT
XR_002958077.1:n.1038-262_1038-257delinsAAATAT
XR_002958078.1:n.875-262_875-257delinsAAATAT
NM_032322.4:c.770-262_770-257delinsAAATAT MANE Select	NP_115698.3:n.770-262_770-257delinsAAATAT
NM_001184992.2:c.835-262_835-257delinsAAATAT	NP_001171921.1:n.835-262_835-257delinsAAATAT
NM_197939.2:c.607-262_607-257delinsAAATAT	NP_922921.1:n.607-262_607-257delinsAAATAT