Canonical Allele Identifier: CA1499093405
Gene: RNF150 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141084357_141084369delinsAATAAAGAGTTTT , CM000666.2:g.141084357_141084369delinsAATAAAGAGTTTT GRCh38
NC_000004.11:g.142005511_142005523delinsAATAAAGAGTTTT , CM000666.1:g.142005511_142005523delinsAATAAAGAGTTTT GRCh37
NC_000004.10:g.142224961_142224973delinsAATAAAGAGTTTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000506101.2:c.-101+47956_-101+47968delinsAAAACTCTTTATT ENSP00000425947.2:n.-101+47956_-101+47968...
ENST00000515673.7:c.484+47956_484+47968delinsAAAACTCTTTATT MANE Select ENSP00000425840.1:n.484+47956_484+47968de...
ENST00000306799.7:c.484+47956_484+47968delinsAAAACTCTTTATT ENSP00000304321.3:n.484+47956_484+47968de...
ENST00000420921.6:c.-5-30638_-5-30626delinsAAAACTCTTTATT ENSP00000394581.2:n.-5-30638_-5-30626deli...
ENST00000507500.5:c.484+47956_484+47968delinsAAAACTCTTTATT ENSP00000425568.1:n.484+47956_484+47968de...
ENST00000515673.6:c.484+47956_484+47968delinsAAAACTCTTTATT ENSP00000425840.1:n.484+47956_484+47968de...
NM_020724.1:c.484+47956_484+47968delinsAAAACTCTTTATT NP_065775.1:n.484+47956_484+47968delinsAA...
XM_005263150.3:c.485-30638_485-30626delinsAAAACTCTTTATT XP_005263207.1:n.485-30638_485-30626delin...
XM_011532147.1:c.34+25505_34+25517delinsAAAACTCTTTATT XP_011530449.1:n.34+25505_34+25517delinsA...
XM_011532148.1:c.-5-30638_-5-30626delinsAAAACTCTTTATT XP_011530450.1:n.-5-30638_-5-30626delinsA...
XM_005263150.5:c.485-30638_485-30626delinsAAAACTCTTTATT XP_005263207.1:n.485-30638_485-30626delin...
XM_011532147.2:c.34+25505_34+25517delinsAAAACTCTTTATT XP_011530449.1:n.34+25505_34+25517delinsA...
XM_011532148.3:c.-5-30638_-5-30626delinsAAAACTCTTTATT XP_011530450.1:n.-5-30638_-5-30626delinsA...
XM_017008475.1:c.34+25505_34+25517delinsAAAACTCTTTATT XP_016863964.1:n.34+25505_34+25517delinsA...
NM_020724.2:c.484+47956_484+47968delinsAAAACTCTTTATT MANE Select NP_065775.1:n.484+47956_484+47968delinsAA...