Canonical Allele Identifier: CA1431675817

Gene: RNF168

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.196487470T= , CM000665.2:g.196487470T=	GRCh38
NC_000003.11:g.196214341T= , CM000665.1:g.196214341T=	GRCh37
NC_000003.10:g.197698738T=	NCBI36
NG_023425.1:g.21299A= , LRG_185:g.21299A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318037.3:c.487A= MANE Select	ENSP00000320898.3:p.Lys163=
ENST00000437070.1:c.*59A=	ENSP00000396712.1:n.*59A=
NM_152617.3:c.487A= , LRG_185t1:c.487A=	NP_689830.2:p.Lys163=
NM_152617.4:c.487A= MANE Select	NP_689830.2:p.Lys163=