Canonical Allele Identifier: CA1499093412
Gene: RNF150 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141084359_141084363delinsTAAAG , CM000666.2:g.141084359_141084363delinsTAAAG GRCh38
NC_000004.11:g.142005513_142005517delinsTAAAG , CM000666.1:g.142005513_142005517delinsTAAAG GRCh37
NC_000004.10:g.142224963_142224967delinsTAAAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000506101.2:c.-101+47962_-101+47966delinsCTTTA ENSP00000425947.2:n.-101+47962_-101+47966...
ENST00000515673.7:c.484+47962_484+47966delinsCTTTA MANE Select ENSP00000425840.1:n.484+47962_484+47966de...
ENST00000306799.7:c.484+47962_484+47966delinsCTTTA ENSP00000304321.3:n.484+47962_484+47966de...
ENST00000420921.6:c.-5-30632_-5-30628delinsCTTTA ENSP00000394581.2:n.-5-30632_-5-30628deli...
ENST00000507500.5:c.484+47962_484+47966delinsCTTTA ENSP00000425568.1:n.484+47962_484+47966de...
ENST00000515673.6:c.484+47962_484+47966delinsCTTTA ENSP00000425840.1:n.484+47962_484+47966de...
NM_020724.1:c.484+47962_484+47966delinsCTTTA NP_065775.1:n.484+47962_484+47966delinsCT...
XM_005263150.3:c.485-30632_485-30628delinsCTTTA XP_005263207.1:n.485-30632_485-30628delin...
XM_011532147.1:c.34+25511_34+25515delinsCTTTA XP_011530449.1:n.34+25511_34+25515delinsC...
XM_011532148.1:c.-5-30632_-5-30628delinsCTTTA XP_011530450.1:n.-5-30632_-5-30628delinsC...
XM_005263150.5:c.485-30632_485-30628delinsCTTTA XP_005263207.1:n.485-30632_485-30628delin...
XM_011532147.2:c.34+25511_34+25515delinsCTTTA XP_011530449.1:n.34+25511_34+25515delinsC...
XM_011532148.3:c.-5-30632_-5-30628delinsCTTTA XP_011530450.1:n.-5-30632_-5-30628delinsC...
XM_017008475.1:c.34+25511_34+25515delinsCTTTA XP_016863964.1:n.34+25511_34+25515delinsC...
NM_020724.2:c.484+47962_484+47966delinsCTTTA MANE Select NP_065775.1:n.484+47962_484+47966delinsCT...