Canonical Allele Identifier: CA2758898520
Gene: CLRN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.150941723_150941724insATAGTCATCGGGGAAGAGGGGGCGCAGAGCACGGTCCACAAGACGGCACGTCAA , CM000665.2:g.150941723_150941724insATAGTCATCGGGGAAGAGGGGGCGCAGAGCACGGTCCACAAGACGGCACGTCAA GRCh38
NC_000003.11:g.150659510_150659511insATAGTCATCGGGGAAGAGGGGGCGCAGAGCACGGTCCACAAGACGGCACGTCAA , CM000665.1:g.150659510_150659511insATAGTCATCGGGGAAGAGGGGGCGCAGAGCACGGTCCACAAGACGGCACGTCAA GRCh37
NC_000003.10:g.152142200_152142201insATAGTCATCGGGGAAGAGGGGGCGCAGAGCACGGTCCACAAGACGGCACGTCAA NCBI36
NG_009168.1:g.36276_36277insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT , LRG_700:g.36276_36277insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000327047.6:c.291_292insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT MANE Select ENSP00000322280.1:p.Ile97_His98insLeuThrCysArgLeuValAspArgAla...
ENST00000468836.2:c.439_440insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT ENSP00000419892.2:p.Pro147LeufsTer17
ENST00000644099.1:c.283_284insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT ENSP00000494762.1:n.283_284insTTGACGTGCCGTCTTGTGGACCGTGCTCTGC...
ENST00000295911.6:c.63_64insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT ENSP00000295911.2:p.Ile21_His22insLeuThrCysArgLeuValAspArgAla...
ENST00000327047.5:c.291_292insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT ENSP00000322280.1:p.Ile97_His98insLeuThrCysArgLeuValAspArgAla...
ENST00000328863.8:c.291_292insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT ENSP00000329158.4:p.Ile97_His98insLeuThrCysArgLeuValAspArgAla...
ENST00000468836.1:c.63_64insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT ENSP00000419892.1:p.Ile21_His22insLeuThrCysArgLeuValAspArgAla...
ENST00000472224.1:n.297_298insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT
ENST00000485607.1:c.-46_-45insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT ENSP00000419244.1:n.-46_-45insTTGACGTGCCGTCTTGTGGACCGTGCTCTGC...
ENST00000565169.1:c.20_21insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT
ENST00000569170.5:c.20_21insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT
NM_001195794.1:c.291_292insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT , LRG_700t1:c.291_292insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT NP_001182723.1:p.Ile97_His98insLeuThrCysArgLeuValAspArgAlaLeu...
NM_001256819.1:c.463_464insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT NP_001243748.1:p.Pro155LeufsTer17
NM_052995.2:c.63_64insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT , LRG_700t2:c.63_64insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT NP_443721.1:p.Ile21_His22insLeuThrCysArgLeuValAspArgAlaLeuArg...
NM_174878.2:c.291_292insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT NP_777367.1:p.Ile97_His98insLeuThrCysArgLeuValAspArgAlaLeuArg...
NR_046380.2:n.733_734insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT
XR_924167.1:n.603_604insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT
NM_001256819.2:c.463_464insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT NP_001243748.1:p.Pro155LeufsTer17
NM_174878.3:c.291_292insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT MANE Select NP_777367.1:p.Ile97_His98insLeuThrCysArgLeuValAspArgAlaLeuArg...
NR_046380.3:n.461_462insTTGACGTGCCGTCTTGTGGACCGTGCTCTGCGCCCCCTCTTCCCCGATGACTAT