Canonical Allele Identifier: CA1499093486

Gene: RNF150

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141084467A= , CM000666.2:g.141084467A=	GRCh38
NC_000004.11:g.142005621A= , CM000666.1:g.142005621A=	GRCh37
NC_000004.10:g.142225071A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000506101.2:c.-101+47858T=	ENSP00000425947.2:n.-101+47858T=
ENST00000515673.7:c.484+47858T= MANE Select	ENSP00000425840.1:n.484+47858T=
ENST00000306799.7:c.484+47858T=	ENSP00000304321.3:n.484+47858T=
ENST00000420921.6:c.-5-30736T=	ENSP00000394581.2:n.-5-30736T=
ENST00000507500.5:c.484+47858T=	ENSP00000425568.1:n.484+47858T=
ENST00000515673.6:c.484+47858T=	ENSP00000425840.1:n.484+47858T=
NM_020724.1:c.484+47858T=	NP_065775.1:n.484+47858T=
XM_005263150.3:c.485-30736T=	XP_005263207.1:n.485-30736T=
XM_011532147.1:c.34+25407T=	XP_011530449.1:n.34+25407T=
XM_011532148.1:c.-5-30736T=	XP_011530450.1:n.-5-30736T=
XM_005263150.5:c.485-30736T=	XP_005263207.1:n.485-30736T=
XM_011532147.2:c.34+25407T=	XP_011530449.1:n.34+25407T=
XM_011532148.3:c.-5-30736T=	XP_011530450.1:n.-5-30736T=
XM_017008475.1:c.34+25407T=	XP_016863964.1:n.34+25407T=
NM_020724.2:c.484+47858T= MANE Select	NP_065775.1:n.484+47858T=