Canonical Allele Identifier: CA1499093421

Gene: RNF150

Linked Data

• dbSNP Id: rs1738270658

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141084372_141084373insT , CM000666.2:g.141084372_141084373insT	GRCh38
NC_000004.11:g.142005526_142005527insT , CM000666.1:g.142005526_142005527insT	GRCh37
NC_000004.10:g.142224976_142224977insT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000506101.2:c.-101+47952_-101+47953insA	ENSP00000425947.2:n.-101+47952_-101+47953...
ENST00000515673.7:c.484+47952_484+47953insA MANE Select	ENSP00000425840.1:n.484+47952_484+47953in...
ENST00000306799.7:c.484+47952_484+47953insA	ENSP00000304321.3:n.484+47952_484+47953in...
ENST00000420921.6:c.-5-30642_-5-30641insA	ENSP00000394581.2:n.-5-30642_-5-30641insA...
ENST00000507500.5:c.484+47952_484+47953insA	ENSP00000425568.1:n.484+47952_484+47953in...
ENST00000515673.6:c.484+47952_484+47953insA	ENSP00000425840.1:n.484+47952_484+47953in...
NM_020724.1:c.484+47952_484+47953insA	NP_065775.1:n.484+47952_484+47953insA
XM_005263150.3:c.485-30642_485-30641insA	XP_005263207.1:n.485-30642_485-30641insA
XM_011532147.1:c.34+25501_34+25502insA	XP_011530449.1:n.34+25501_34+25502insA
XM_011532148.1:c.-5-30642_-5-30641insA	XP_011530450.1:n.-5-30642_-5-30641insA
XM_005263150.5:c.485-30642_485-30641insA	XP_005263207.1:n.485-30642_485-30641insA
XM_011532147.2:c.34+25501_34+25502insA	XP_011530449.1:n.34+25501_34+25502insA
XM_011532148.3:c.-5-30642_-5-30641insA	XP_011530450.1:n.-5-30642_-5-30641insA
XM_017008475.1:c.34+25501_34+25502insA	XP_016863964.1:n.34+25501_34+25502insA
NM_020724.2:c.484+47952_484+47953insA MANE Select	NP_065775.1:n.484+47952_484+47953insA