Canonical Allele Identifier: CA1499093444

Gene: RNF150

Linked Data

• dbSNP Id: rs1001665653

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141084403T>G , CM000666.2:g.141084403T>G	GRCh38
NC_000004.11:g.142005557T>G , CM000666.1:g.142005557T>G	GRCh37
NC_000004.10:g.142225007T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506101.2:c.-101+47922A>C	ENSP00000425947.2:n.-101+47922A>C
ENST00000515673.7:c.484+47922A>C MANE Select	ENSP00000425840.1:n.484+47922A>C
ENST00000306799.7:c.484+47922A>C	ENSP00000304321.3:n.484+47922A>C
ENST00000420921.6:c.-5-30672A>C	ENSP00000394581.2:n.-5-30672A>C
ENST00000507500.5:c.484+47922A>C	ENSP00000425568.1:n.484+47922A>C
ENST00000515673.6:c.484+47922A>C	ENSP00000425840.1:n.484+47922A>C
NM_020724.1:c.484+47922A>C	NP_065775.1:n.484+47922A>C
XM_005263150.3:c.485-30672A>C	XP_005263207.1:n.485-30672A>C
XM_011532147.1:c.34+25471A>C	XP_011530449.1:n.34+25471A>C
XM_011532148.1:c.-5-30672A>C	XP_011530450.1:n.-5-30672A>C
XM_005263150.5:c.485-30672A>C	XP_005263207.1:n.485-30672A>C
XM_011532147.2:c.34+25471A>C	XP_011530449.1:n.34+25471A>C
XM_011532148.3:c.-5-30672A>C	XP_011530450.1:n.-5-30672A>C
XM_017008475.1:c.34+25471A>C	XP_016863964.1:n.34+25471A>C
NM_020724.2:c.484+47922A>C MANE Select	NP_065775.1:n.484+47922A>C