Canonical Allele Identifier: CA1499093445

Gene: RNF150

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141084405_141084409delinsGATTA , CM000666.2:g.141084405_141084409delinsGATTA	GRCh38
NC_000004.11:g.142005559_142005563delinsGATTA , CM000666.1:g.142005559_142005563delinsGATTA	GRCh37
NC_000004.10:g.142225009_142225013delinsGATTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506101.2:c.-101+47916_-101+47920delinsTAATC	ENSP00000425947.2:n.-101+47916_-101+47920delinsTAATC
ENST00000515673.7:c.484+47916_484+47920delinsTAATC MANE Select	ENSP00000425840.1:n.484+47916_484+47920delinsTAATC
ENST00000306799.7:c.484+47916_484+47920delinsTAATC	ENSP00000304321.3:n.484+47916_484+47920delinsTAATC
ENST00000420921.6:c.-5-30678_-5-30674delinsTAATC	ENSP00000394581.2:n.-5-30678_-5-30674delinsTAATC
ENST00000507500.5:c.484+47916_484+47920delinsTAATC	ENSP00000425568.1:n.484+47916_484+47920delinsTAATC
ENST00000515673.6:c.484+47916_484+47920delinsTAATC	ENSP00000425840.1:n.484+47916_484+47920delinsTAATC
NM_020724.1:c.484+47916_484+47920delinsTAATC	NP_065775.1:n.484+47916_484+47920delinsTAATC
XM_005263150.3:c.485-30678_485-30674delinsTAATC	XP_005263207.1:n.485-30678_485-30674delinsTAATC
XM_011532147.1:c.34+25465_34+25469delinsTAATC	XP_011530449.1:n.34+25465_34+25469delinsTAATC
XM_011532148.1:c.-5-30678_-5-30674delinsTAATC	XP_011530450.1:n.-5-30678_-5-30674delinsTAATC
XM_005263150.5:c.485-30678_485-30674delinsTAATC	XP_005263207.1:n.485-30678_485-30674delinsTAATC
XM_011532147.2:c.34+25465_34+25469delinsTAATC	XP_011530449.1:n.34+25465_34+25469delinsTAATC
XM_011532148.3:c.-5-30678_-5-30674delinsTAATC	XP_011530450.1:n.-5-30678_-5-30674delinsTAATC
XM_017008475.1:c.34+25465_34+25469delinsTAATC	XP_016863964.1:n.34+25465_34+25469delinsTAATC
NM_020724.2:c.484+47916_484+47920delinsTAATC MANE Select	NP_065775.1:n.484+47916_484+47920delinsTAATC