Canonical Allele Identifier: CA1499093422

Gene: RNF150

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141084373_141084374delinsCT , CM000666.2:g.141084373_141084374delinsCT	GRCh38
NC_000004.11:g.142005527_142005528delinsCT , CM000666.1:g.142005527_142005528delinsCT	GRCh37
NC_000004.10:g.142224977_142224978delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000506101.2:c.-101+47951_-101+47952delinsAG	ENSP00000425947.2:n.-101+47951_-101+47952...
ENST00000515673.7:c.484+47951_484+47952delinsAG MANE Select	ENSP00000425840.1:n.484+47951_484+47952de...
ENST00000306799.7:c.484+47951_484+47952delinsAG	ENSP00000304321.3:n.484+47951_484+47952de...
ENST00000420921.6:c.-5-30643_-5-30642delinsAG	ENSP00000394581.2:n.-5-30643_-5-30642deli...
ENST00000507500.5:c.484+47951_484+47952delinsAG	ENSP00000425568.1:n.484+47951_484+47952de...
ENST00000515673.6:c.484+47951_484+47952delinsAG	ENSP00000425840.1:n.484+47951_484+47952de...
NM_020724.1:c.484+47951_484+47952delinsAG	NP_065775.1:n.484+47951_484+47952delinsAG...
XM_005263150.3:c.485-30643_485-30642delinsAG	XP_005263207.1:n.485-30643_485-30642delin...
XM_011532147.1:c.34+25500_34+25501delinsAG	XP_011530449.1:n.34+25500_34+25501delinsA...
XM_011532148.1:c.-5-30643_-5-30642delinsAG	XP_011530450.1:n.-5-30643_-5-30642delinsA...
XM_005263150.5:c.485-30643_485-30642delinsAG	XP_005263207.1:n.485-30643_485-30642delin...
XM_011532147.2:c.34+25500_34+25501delinsAG	XP_011530449.1:n.34+25500_34+25501delinsA...
XM_011532148.3:c.-5-30643_-5-30642delinsAG	XP_011530450.1:n.-5-30643_-5-30642delinsA...
XM_017008475.1:c.34+25500_34+25501delinsAG	XP_016863964.1:n.34+25500_34+25501delinsA...
NM_020724.2:c.484+47951_484+47952delinsAG MANE Select	NP_065775.1:n.484+47951_484+47952delinsAG...