Canonical Allele Identifier: CA2539620615
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618716_151618717insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT , CM000668.2:g.151618716_151618717insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT GRCh38
NC_000006.11:g.151939851_151939852insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT , CM000668.1:g.151939851_151939852insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT GRCh37
NC_000006.10:g.151981544_151981545insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT NCBI36
NG_021198.1:g.129677_129678insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT MANE Select ENSP00000239374.6:n.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACAT...
ENST00000239374.7:c.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT ENSP00000239374.6:n.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACAT...
NM_025059.3:c.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT NP_079335.2:n.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCA...
XM_011536147.1:c.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT XP_011534449.1:n.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCT...
XM_011536148.1:c.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT XP_011534450.1:n.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCT...
XM_011536147.2:c.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT XP_011534449.1:n.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCT...
XM_011536148.2:c.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT XP_011534450.1:n.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCT...
NM_025059.4:c.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCATAAGGTCGCGGTTGACGAAGATCTCGTGCTCCTCGAGCACCCGCTTCAGATACGGATGATCCTCCACACGCAGCGAGCGCGGCAGCTCGT MANE Select NP_079335.2:n.*569_*570insGACAATCGGTGCGGCAAGATCAGGAACATTCTTCA...