Canonical Allele Identifier: CA107365181

Gene: RNF150

Linked Data

• dbSNP Id: rs554531121
• gnomAD v3: 4-141084376-T-C
• gnomAD v4: 4-141084376-T-C
• MyVariant Identifiers: chr4:g.142005530T>C (hg19) ; chr4:g.141084376T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141084376T>C , CM000666.2:g.141084376T>C	GRCh38
NC_000004.11:g.142005530T>C , CM000666.1:g.142005530T>C	GRCh37
NC_000004.10:g.142224980T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000506101.2:c.-101+47949A>G	ENSP00000425947.2:n.-101+47949A>G
ENST00000515673.7:c.484+47949A>G MANE Select	ENSP00000425840.1:n.484+47949A>G
ENST00000306799.7:c.484+47949A>G	ENSP00000304321.3:n.484+47949A>G
ENST00000420921.6:c.-5-30645A>G	ENSP00000394581.2:n.-5-30645A>G
ENST00000507500.5:c.484+47949A>G	ENSP00000425568.1:n.484+47949A>G
ENST00000515673.6:c.484+47949A>G	ENSP00000425840.1:n.484+47949A>G
NM_020724.1:c.484+47949A>G	NP_065775.1:n.484+47949A>G
XM_005263150.3:c.485-30645A>G	XP_005263207.1:n.485-30645A>G
XM_011532147.1:c.34+25498A>G	XP_011530449.1:n.34+25498A>G
XM_011532148.1:c.-5-30645A>G	XP_011530450.1:n.-5-30645A>G
XM_005263150.5:c.485-30645A>G	XP_005263207.1:n.485-30645A>G
XM_011532147.2:c.34+25498A>G	XP_011530449.1:n.34+25498A>G
XM_011532148.3:c.-5-30645A>G	XP_011530450.1:n.-5-30645A>G
XM_017008475.1:c.34+25498A>G	XP_016863964.1:n.34+25498A>G
NM_020724.2:c.484+47949A>G MANE Select	NP_065775.1:n.484+47949A>G