Canonical Allele Identifier: CA1095909488
Gene: CCDC170 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151526652_151526653insCTAGAGGTGTGCACCACCATGC , CM000668.2:g.151526652_151526653insCTAGAGGTGTGCACCACCATGC GRCh38
NC_000006.11:g.151847787_151847788insCTAGAGGTGTGCACCACCATGC , CM000668.1:g.151847787_151847788insCTAGAGGTGTGCACCACCATGC GRCh37
NC_000006.10:g.151889480_151889481insCTAGAGGTGTGCACCACCATGC NCBI36
NG_021198.1:g.37613_37614insCTAGAGGTGTGCACCACCATGC

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.8:c.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC MANE Select ENSP00000239374.6:n.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC
ENST00000239374.7:c.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC ENSP00000239374.6:n.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC
NM_025059.3:c.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC NP_079335.2:n.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC
NM_025059.4:c.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC MANE Select NP_079335.2:n.58-9666_58-9665insCTAGAGGTGTGCACCACCATGC