Canonical Allele Identifier: CA355625476
Gene: RNF168 HGNC NCBI

Linked Data

COSMIC: COSM6340773
MyVariant Identifiers: chr3:g.196214389G>T (hg19) chr3:g.196487518G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487518G>T , CM000665.2:g.196487518G>T GRCh38
NC_000003.11:g.196214389G>T , CM000665.1:g.196214389G>T GRCh37
NC_000003.10:g.197698786G>T NCBI36
NG_023425.1:g.21251C>A , LRG_185:g.21251C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.439C>A MANE Select ENSP00000320898.3:p.Gln147Lys
ENST00000437070.1:c.*11C>A ENSP00000396712.1:n.*11C>A
NM_152617.3:c.439C>A , LRG_185t1:c.439C>A NP_689830.2:p.Gln147Lys
NM_152617.4:c.439C>A MANE Select NP_689830.2:p.Gln147Lys
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