Canonical Allele Identifier: CA2778230555
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143321344_143321345insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG , CM000669.2:g.143321344_143321345insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG GRCh38
NC_000007.13:g.143018437_143018438insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG , CM000669.1:g.143018437_143018438insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG GRCh37
NC_000007.12:g.142728559_142728560insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG NCBI36
NG_009815.1:g.10219_10220insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG
NG_009815.2:g.10219_10220insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000650516.2:c.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG ENSP00000498052.2:n.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGT...
ENST00000343257.7:c.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG MANE Select ENSP00000339867.2:n.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGT...
ENST00000432192.6:c.202-21_202-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG
ENST00000650516.1:c.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG ENSP00000498052.1:n.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGT...
ENST00000343257.6:c.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG ENSP00000339867.2:n.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGT...
NM_000083.2:c.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG NP_000074.2:n.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGG...
NR_046453.1:n.521-21_521-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG
XM_011515781.1:c.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG XP_011514083.1:n.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGTAGC...
XM_017011739.1:c.141-21_141-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG XP_016867228.1:n.141-21_141-20insGCAAGAACCCAGCGCGTTTATCGGTAGC...
XM_017011740.1:c.141-21_141-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG XP_016867229.1:n.141-21_141-20insGCAAGAACCCAGCGCGTTTATCGGTAGC...
NM_000083.3:c.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG MANE Select NP_000074.3:n.434-21_434-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGG...
NR_046453.2:n.536-21_536-20insGCAAGAACCCAGCGCGTTTATCGGTAGCAGGGTCAATAATGGTCTTACGGTTGCGCCAAGCATCTCGGACGTGCGCACCACCAAGGGCACCAAGAACGTTAGCACGGACAGAG