Canonical Allele Identifier: CA2368296996

Gene: RNF114

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49938091C= , CM000682.2:g.49938091C=	GRCh38
NC_000020.10:g.48554628C= , CM000682.1:g.48554628C=	GRCh37
NC_000020.9:g.47988035C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244061.6:c.140+1539C= MANE Select	ENSP00000244061.2:n.140+1539C=
ENST00000244061.5:c.140+1539C=	ENSP00000244061.2:n.140+1539C=
ENST00000622920.1:c.140+1539C=	ENSP00000485317.1:n.140+1539C=
ENST00000622999.3:c.140+1539C=	ENSP00000485203.1:n.140+1539C=
ENST00000623528.3:c.140+1539C=	ENSP00000485136.1:n.140+1539C=
ENST00000623732.3:c.140+1539C=	ENSP00000485575.1:n.140+1539C=
ENST00000624620.1:n.154+1539C=
ENST00000625177.3:c.140+1539C=	ENSP00000485239.1:n.140+1539C=
NM_018683.3:c.140+1539C=	NP_061153.1:n.140+1539C=
NM_018683.4:c.140+1539C= MANE Select	NP_061153.1:n.140+1539C=