Canonical Allele Identifier: CA788154246

Gene: RNF150

Linked Data

• dbSNP Id: rs1441746121
• MyVariant Identifiers: chr4:g.142005472_142005485del (hg19) ; chr4:g.141084318_141084331del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141084320_141084333del , CM000666.2:g.141084320_141084333del	GRCh38
NC_000004.11:g.142005474_142005487del , CM000666.1:g.142005474_142005487del	GRCh37
NC_000004.10:g.142224924_142224937del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000506101.2:c.-101+47994_-101+48007del	ENSP00000425947.2:n.-101+47994_-101+48007...
ENST00000515673.7:c.484+47994_484+48007del MANE Select	ENSP00000425840.1:n.484+47994_484+48007de...
ENST00000306799.7:c.484+47994_484+48007del	ENSP00000304321.3:n.484+47994_484+48007de...
ENST00000420921.6:c.-5-30600_-5-30587del	ENSP00000394581.2:n.-5-30600_-5-30587del
ENST00000507500.5:c.484+47994_484+48007del	ENSP00000425568.1:n.484+47994_484+48007de...
ENST00000515673.6:c.484+47994_484+48007del	ENSP00000425840.1:n.484+47994_484+48007de...
NM_020724.1:c.484+47994_484+48007del	NP_065775.1:n.484+47994_484+48007del
XM_005263150.3:c.485-30600_485-30587del	XP_005263207.1:n.485-30600_485-30587del
XM_011532147.1:c.34+25543_34+25556del	XP_011530449.1:n.34+25543_34+25556del
XM_011532148.1:c.-5-30600_-5-30587del	XP_011530450.1:n.-5-30600_-5-30587del
XM_005263150.5:c.485-30600_485-30587del	XP_005263207.1:n.485-30600_485-30587del
XM_011532147.2:c.34+25543_34+25556del	XP_011530449.1:n.34+25543_34+25556del
XM_011532148.3:c.-5-30600_-5-30587del	XP_011530450.1:n.-5-30600_-5-30587del
XM_017008475.1:c.34+25543_34+25556del	XP_016863964.1:n.34+25543_34+25556del
NM_020724.2:c.484+47994_484+48007del MANE Select	NP_065775.1:n.484+47994_484+48007del