Canonical Allele Identifier: CA2552284890

Gene: RNF150

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141084222_141084223insGAGCATAATTTTAATCTTTATTCAGTCTCCATTTATGC , CM000666.2:g.141084222_141084223insGAGCATAATTTTAATCTTTATTCAGTCTCCATTTATGC	GRCh38
NC_000004.11:g.142005376_142005377insGAGCATAATTTTAATCTTTATTCAGTCTCCATTTATGC , CM000666.1:g.142005376_142005377insGAGCATAATTTTAATCTTTATTCAGTCTCCATTTATGC	GRCh37
NC_000004.10:g.142224826_142224827insGAGCATAATTTTAATCTTTATTCAGTCTCCATTTATGC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000506101.2:c.-101+48102_-101+48103insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	ENSP00000425947.2:n.-101+48102_-101+48103insGCATAAATGGAGACTGA...
ENST00000515673.7:c.484+48102_484+48103insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC MANE Select	ENSP00000425840.1:n.484+48102_484+48103insGCATAAATGGAGACTGAAT...
ENST00000306799.7:c.484+48102_484+48103insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	ENSP00000304321.3:n.484+48102_484+48103insGCATAAATGGAGACTGAAT...
ENST00000420921.6:c.-5-30492_-5-30491insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	ENSP00000394581.2:n.-5-30492_-5-30491insGCATAAATGGAGACTGAATAA...
ENST00000507500.5:c.484+48102_484+48103insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	ENSP00000425568.1:n.484+48102_484+48103insGCATAAATGGAGACTGAAT...
ENST00000515673.6:c.484+48102_484+48103insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	ENSP00000425840.1:n.484+48102_484+48103insGCATAAATGGAGACTGAAT...
NM_020724.1:c.484+48102_484+48103insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	NP_065775.1:n.484+48102_484+48103insGCATAAATGGAGACTGAATAAAGAT...
XM_005263150.3:c.485-30492_485-30491insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	XP_005263207.1:n.485-30492_485-30491insGCATAAATGGAGACTGAATAAA...
XM_011532147.1:c.34+25651_34+25652insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	XP_011530449.1:n.34+25651_34+25652insGCATAAATGGAGACTGAATAAAGA...
XM_011532148.1:c.-5-30492_-5-30491insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	XP_011530450.1:n.-5-30492_-5-30491insGCATAAATGGAGACTGAATAAAGA...
XM_005263150.5:c.485-30492_485-30491insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	XP_005263207.1:n.485-30492_485-30491insGCATAAATGGAGACTGAATAAA...
XM_011532147.2:c.34+25651_34+25652insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	XP_011530449.1:n.34+25651_34+25652insGCATAAATGGAGACTGAATAAAGA...
XM_011532148.3:c.-5-30492_-5-30491insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	XP_011530450.1:n.-5-30492_-5-30491insGCATAAATGGAGACTGAATAAAGA...
XM_017008475.1:c.34+25651_34+25652insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC	XP_016863964.1:n.34+25651_34+25652insGCATAAATGGAGACTGAATAAAGA...
NM_020724.2:c.484+48102_484+48103insGCATAAATGGAGACTGAATAAAGATTAAAATTATGCTC MANE Select	NP_065775.1:n.484+48102_484+48103insGCATAAATGGAGACTGAATAAAGAT...