Canonical Allele Identifier: CA2793833657
Gene: C1QTNF5 HGNC NCBI
MFRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119339423_119339424insTATGACTATCTCGAACGGAATGCCACTGATGAGGATAAAGTGGCAGGACTGGACATCGCAGATTTCCTTCTACGGCAAATGCCCAACCTGAAAGTACCATCTGCAAAAGCTGATGAAGGAGT , CM000673.2:g.119339423_119339424insTATGACTATCTCGAACGGAATGCCACTGATGAGGATAAAGTGGCAGGACTGGACATCGCAGATTTCCTTCTACGGCAAATGCCCAACCTGAAAGTACCATCTGCAAAAGCTGATGAAGGAGT GRCh38
NC_000011.9:g.119210133_119210134insTATGACTATCTCGAACGGAATGCCACTGATGAGGATAAAGTGGCAGGACTGGACATCGCAGATTTCCTTCTACGGCAAATGCCCAACCTGAAAGTACCATCTGCAAAAGCTGATGAAGGAGT , CM000673.1:g.119210133_119210134insTATGACTATCTCGAACGGAATGCCACTGATGAGGATAAAGTGGCAGGACTGGACATCGCAGATTTCCTTCTACGGCAAATGCCCAACCTGAAAGTACCATCTGCAAAAGCTGATGAAGGAGT GRCh37
NC_000011.8:g.118715343_118715344insTATGACTATCTCGAACGGAATGCCACTGATGAGGATAAAGTGGCAGGACTGGACATCGCAGATTTCCTTCTACGGCAAATGCCCAACCTGAAAGTACCATCTGCAAAAGCTGATGAAGGAGT NCBI36
NG_012235.1:g.12250_12251insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000528368.3:c.639_640insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (C1QTNF5) MANE Select ENSP00000431140.1:p.Tyr214ThrfsTer39
ENST00000619721.6:c.*1535_*1536insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (MFRP) MANE Select ENSP00000481824.1:n.*1535_*1536insACTCCTTCATCAGCTTTTGCAGATGGT...
ENST00000525657.2:n.529_530insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (C1QTNF5)
ENST00000528368.2:c.639_640insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (C1QTNF5) ENSP00000431140.1:p.Tyr214ThrfsTer39
ENST00000530681.2:c.639_640insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (C1QTNF5) ENSP00000456533.2:p.Tyr214ThrfsTer39
ENST00000619721.5:c.*1535_*1536insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (MFRP) ENSP00000481824.1:n.*1535_*1536insACTCCTTCATCAGCTTTTGCAGATGGT...
NM_001278431.1:c.639_640insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (C1QTNF5) NP_001265360.1:p.Tyr214ThrfsTer39
NM_015645.4:c.639_640insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (C1QTNF5) NP_056460.1:p.Tyr214ThrfsTer39
NM_031433.3:c.*1535_*1536insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (MFRP) NP_113621.1:n.*1535_*1536insACTCCTTCATCAGCTTTTGCAGATGGTACTTTC...
NM_001278431.2:c.639_640insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (C1QTNF5) MANE Select NP_001265360.1:p.Tyr214ThrfsTer39
NM_031433.4:c.*1535_*1536insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (MFRP) MANE Select NP_113621.1:n.*1535_*1536insACTCCTTCATCAGCTTTTGCAGATGGTACTTTC...
NM_015645.5:c.639_640insACTCCTTCATCAGCTTTTGCAGATGGTACTTTCAGGTTGGGCATTTGCCGTAGAAGGAAATCTGCGATGTCCAGTCCTGCCACTTTATCCTCATCAGTGGCATTCCGTTCGAGATAGTCATA (C1QTNF5) NP_056460.1:p.Tyr214ThrfsTer39