Canonical Allele Identifier: CA1499093341

Gene: RNF150

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.141084264_141084265delinsCA , CM000666.2:g.141084264_141084265delinsCA	GRCh38
NC_000004.11:g.142005418_142005419delinsCA , CM000666.1:g.142005418_142005419delinsCA	GRCh37
NC_000004.10:g.142224868_142224869delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000506101.2:c.-101+48060_-101+48061delinsTG	ENSP00000425947.2:n.-101+48060_-101+48061delinsTG
ENST00000515673.7:c.484+48060_484+48061delinsTG MANE Select	ENSP00000425840.1:n.484+48060_484+48061delinsTG
ENST00000306799.7:c.484+48060_484+48061delinsTG	ENSP00000304321.3:n.484+48060_484+48061delinsTG
ENST00000420921.6:c.-5-30534_-5-30533delinsTG	ENSP00000394581.2:n.-5-30534_-5-30533delinsTG
ENST00000507500.5:c.484+48060_484+48061delinsTG	ENSP00000425568.1:n.484+48060_484+48061delinsTG
ENST00000515673.6:c.484+48060_484+48061delinsTG	ENSP00000425840.1:n.484+48060_484+48061delinsTG
NM_020724.1:c.484+48060_484+48061delinsTG	NP_065775.1:n.484+48060_484+48061delinsTG
XM_005263150.3:c.485-30534_485-30533delinsTG	XP_005263207.1:n.485-30534_485-30533delinsTG
XM_011532147.1:c.34+25609_34+25610delinsTG	XP_011530449.1:n.34+25609_34+25610delinsTG
XM_011532148.1:c.-5-30534_-5-30533delinsTG	XP_011530450.1:n.-5-30534_-5-30533delinsTG
XM_005263150.5:c.485-30534_485-30533delinsTG	XP_005263207.1:n.485-30534_485-30533delinsTG
XM_011532147.2:c.34+25609_34+25610delinsTG	XP_011530449.1:n.34+25609_34+25610delinsTG
XM_011532148.3:c.-5-30534_-5-30533delinsTG	XP_011530450.1:n.-5-30534_-5-30533delinsTG
XM_017008475.1:c.34+25609_34+25610delinsTG	XP_016863964.1:n.34+25609_34+25610delinsTG
NM_020724.2:c.484+48060_484+48061delinsTG MANE Select	NP_065775.1:n.484+48060_484+48061delinsTG