Canonical Allele Identifier: CA355625255
Gene: RNF168 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487469T>G , CM000665.2:g.196487469T>G GRCh38
NC_000003.11:g.196214340T>G , CM000665.1:g.196214340T>G GRCh37
NC_000003.10:g.197698737T>G NCBI36
NG_023425.1:g.21300A>C , LRG_185:g.21300A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.488A>C MANE Select ENSP00000320898.3:p.Lys163Thr
ENST00000437070.1:c.*60A>C ENSP00000396712.1:n.*60A>C
NM_152617.3:c.488A>C , LRG_185t1:c.488A>C NP_689830.2:p.Lys163Thr
NM_152617.4:c.488A>C MANE Select NP_689830.2:p.Lys163Thr