Canonical Allele Identifier: CA107365186
Gene: RNF150 HGNC NCBI

Linked Data

dbSNP Id: rs10007052

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.141084419C>A , CM000666.2:g.141084419C>A GRCh38
NC_000004.11:g.142005573C>A , CM000666.1:g.142005573C>A GRCh37
NC_000004.10:g.142225023C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000506101.2:c.-101+47906G>T ENSP00000425947.2:p.=
ENST00000515673.7:c.484+47906G>T MANE Select ENSP00000425840.1:p.=
ENST00000306799.7:c.484+47906G>T ENSP00000304321.3:p.=
ENST00000420921.6:c.-5-30688G>T ENSP00000394581.2:p.=
ENST00000507500.5:c.484+47906G>T ENSP00000425568.1:p.=
ENST00000515673.6:c.484+47906G>T ENSP00000425840.1:p.=
NM_020724.1:c.484+47906G>T NP_065775.1:p.=
XM_005263150.3:c.485-30688G>T XP_005263207.1:p.=
XM_011532147.1:c.34+25455G>T XP_011530449.1:p.=
XM_011532148.1:c.-5-30688G>T XP_011530450.1:p.=
XM_005263150.5:c.485-30688G>T XP_005263207.1:p.=
XM_011532147.2:c.34+25455G>T XP_011530449.1:p.=
XM_011532148.3:c.-5-30688G>T XP_011530450.1:p.=
XM_017008475.1:c.34+25455G>T XP_016863964.1:p.=
NM_020724.2:c.484+47906G>T MANE Select NP_065775.1:p.=