Canonical Allele Identifier: CA1499093379
Gene: RNF150 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141084317_141084331delinsGAATATATAGGATAT , CM000666.2:g.141084317_141084331delinsGAATATATAGGATAT GRCh38
NC_000004.11:g.142005471_142005485delinsGAATATATAGGATAT , CM000666.1:g.142005471_142005485delinsGAATATATAGGATAT GRCh37
NC_000004.10:g.142224921_142224935delinsGAATATATAGGATAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000506101.2:c.-101+47994_-101+48008delinsATATCCTATATATTC ENSP00000425947.2:n.-101+47994_-101+48008...
ENST00000515673.7:c.484+47994_484+48008delinsATATCCTATATATTC MANE Select ENSP00000425840.1:n.484+47994_484+48008de...
ENST00000306799.7:c.484+47994_484+48008delinsATATCCTATATATTC ENSP00000304321.3:n.484+47994_484+48008de...
ENST00000420921.6:c.-5-30600_-5-30586delinsATATCCTATATATTC ENSP00000394581.2:n.-5-30600_-5-30586deli...
ENST00000507500.5:c.484+47994_484+48008delinsATATCCTATATATTC ENSP00000425568.1:n.484+47994_484+48008de...
ENST00000515673.6:c.484+47994_484+48008delinsATATCCTATATATTC ENSP00000425840.1:n.484+47994_484+48008de...
NM_020724.1:c.484+47994_484+48008delinsATATCCTATATATTC NP_065775.1:n.484+47994_484+48008delinsAT...
XM_005263150.3:c.485-30600_485-30586delinsATATCCTATATATTC XP_005263207.1:n.485-30600_485-30586delin...
XM_011532147.1:c.34+25543_34+25557delinsATATCCTATATATTC XP_011530449.1:n.34+25543_34+25557delinsA...
XM_011532148.1:c.-5-30600_-5-30586delinsATATCCTATATATTC XP_011530450.1:n.-5-30600_-5-30586delinsA...
XM_005263150.5:c.485-30600_485-30586delinsATATCCTATATATTC XP_005263207.1:n.485-30600_485-30586delin...
XM_011532147.2:c.34+25543_34+25557delinsATATCCTATATATTC XP_011530449.1:n.34+25543_34+25557delinsA...
XM_011532148.3:c.-5-30600_-5-30586delinsATATCCTATATATTC XP_011530450.1:n.-5-30600_-5-30586delinsA...
XM_017008475.1:c.34+25543_34+25557delinsATATCCTATATATTC XP_016863964.1:n.34+25543_34+25557delinsA...
NM_020724.2:c.484+47994_484+48008delinsATATCCTATATATTC MANE Select NP_065775.1:n.484+47994_484+48008delinsAT...