Canonical Allele Identifier: CA1431675808
Gene: RNF168 HGNC NCBI

Linked Data

dbSNP Id: rs1732483891
gnomAD v4: 3-196487458-C-CTCT
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487461_196487463dup , CM000665.2:g.196487461_196487463dup GRCh38
NC_000003.11:g.196214332_196214334dup , CM000665.1:g.196214332_196214334dup GRCh37
NC_000003.10:g.197698729_197698731dup NCBI36
NG_023425.1:g.21308_21310dup , LRG_185:g.21308_21310dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.496_498dup MANE Select ENSP00000320898.3:p.Arg166_Ala167insArg
ENST00000437070.1:c.*68_*70dup ENSP00000396712.1:n.*68_*70dup
NM_152617.3:c.496_498dup , LRG_185t1:c.496_498dup NP_689830.2:p.Arg166_Ala167insArg
NM_152617.4:c.496_498dup MANE Select NP_689830.2:p.Arg166_Ala167insArg
Search 100 bp 5'
Search 100 bp 3'