Canonical Allele Identifier: CA2707365355

Gene: RNF150

Linked Data

• dbSNP Id: rs2110988705

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141084385G>A , CM000666.2:g.141084385G>A	GRCh38
NC_000004.11:g.142005539G>A , CM000666.1:g.142005539G>A	GRCh37
NC_000004.10:g.142224989G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000506101.2:c.-101+47940C>T	ENSP00000425947.2:n.-101+47940C>T
ENST00000515673.7:c.484+47940C>T MANE Select	ENSP00000425840.1:n.484+47940C>T
ENST00000306799.7:c.484+47940C>T	ENSP00000304321.3:n.484+47940C>T
ENST00000420921.6:c.-5-30654C>T	ENSP00000394581.2:n.-5-30654C>T
ENST00000507500.5:c.484+47940C>T	ENSP00000425568.1:n.484+47940C>T
ENST00000515673.6:c.484+47940C>T	ENSP00000425840.1:n.484+47940C>T
NM_020724.1:c.484+47940C>T	NP_065775.1:n.484+47940C>T
XM_005263150.3:c.485-30654C>T	XP_005263207.1:n.485-30654C>T
XM_011532147.1:c.34+25489C>T	XP_011530449.1:n.34+25489C>T
XM_011532148.1:c.-5-30654C>T	XP_011530450.1:n.-5-30654C>T
XM_005263150.5:c.485-30654C>T	XP_005263207.1:n.485-30654C>T
XM_011532147.2:c.34+25489C>T	XP_011530449.1:n.34+25489C>T
XM_011532148.3:c.-5-30654C>T	XP_011530450.1:n.-5-30654C>T
XM_017008475.1:c.34+25489C>T	XP_016863964.1:n.34+25489C>T
NM_020724.2:c.484+47940C>T MANE Select	NP_065775.1:n.484+47940C>T