Canonical Allele Identifier: CA2255462442

Gene: RNF135

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30998638_30998641delinsATTG , CM000679.2:g.30998638_30998641delinsATTG	GRCh38
NC_000017.10:g.29325656_29325659delinsATTG , CM000679.1:g.29325656_29325659delinsATTG	GRCh37
NC_000017.9:g.26349782_26349785delinsATTG	NCBI36
NG_011701.1:g.32701_32704delinsATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328381.10:c.770-24_770-21delinsATTG MANE Select	ENSP00000328340.5:n.770-24_770-21delinsATTG
ENST00000324689.8:c.607-24_607-21delinsATTG	ENSP00000323693.4:n.607-24_607-21delinsATTG
ENST00000328381.9:c.770-24_770-21delinsATTG	ENSP00000328340.5:n.770-24_770-21delinsATTG
ENST00000443677.6:c.463-24_463-21delinsATTG	ENSP00000411965.2:n.463-24_463-21delinsATTG
ENST00000535306.6:c.835-24_835-21delinsATTG	ENSP00000440470.2:n.835-24_835-21delinsATTG
NM_001184992.1:c.835-24_835-21delinsATTG	NP_001171921.1:n.835-24_835-21delinsATTG
NM_032322.3:c.770-24_770-21delinsATTG	NP_115698.3:n.770-24_770-21delinsATTG
NM_197939.1:c.607-24_607-21delinsATTG	NP_922921.1:n.607-24_607-21delinsATTG
XM_005258043.3:c.227-24_227-21delinsATTG	XP_005258100.1:n.227-24_227-21delinsATTG
XM_006722138.2:c.449-24_449-21delinsATTG	XP_006722201.1:n.449-24_449-21delinsATTG
XM_017025223.1:c.227-24_227-21delinsATTG	XP_016880712.1:n.227-24_227-21delinsATTG
XM_024451000.1:c.227-24_227-21delinsATTG	XP_024306768.1:n.227-24_227-21delinsATTG
XM_024451001.1:c.227-24_227-21delinsATTG	XP_024306769.1:n.227-24_227-21delinsATTG
XR_002958076.1:n.1103-24_1103-21delinsATTG
XR_002958077.1:n.1038-24_1038-21delinsATTG
XR_002958078.1:n.875-24_875-21delinsATTG
NM_032322.4:c.770-24_770-21delinsATTG MANE Select	NP_115698.3:n.770-24_770-21delinsATTG
NM_001184992.2:c.835-24_835-21delinsATTG	NP_001171921.1:n.835-24_835-21delinsATTG
NM_197939.2:c.607-24_607-21delinsATTG	NP_922921.1:n.607-24_607-21delinsATTG