Canonical Allele Identifier: CA2500932266

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316222_13316223insCTAGCTTTTTCATTCCTTGCTTCGCTTCCCATCCTCATGGCTCAAAGGATGAGCCCATTTACCTGAAGGTG , CM000682.2:g.13316222_13316223insCTAGCTTTTTCATTCCTTGCTTCGCTTCCCATCCTCATGGCTCAAAGGATGAGCCCATTTACCTGAAGGTG GRCh38
NC_000020.10:g.13296869_13296870insCTAGCTTTTTCATTCCTTGCTTCGCTTCCCATCCTCATGGCTCAAAGGATGAGCCCATTTACCTGAAGGTG , CM000682.1:g.13296869_13296870insCTAGCTTTTTCATTCCTTGCTTCGCTTCCCATCCTCATGGCTCAAAGGATGAGCCCATTTACCTGAAGGTG GRCh37
NC_000020.9:g.13244869_13244870insCTAGCTTTTTCATTCCTTGCTTCGCTTCCCATCCTCATGGCTCAAAGGATGAGCCCATTTACCTGAAGGTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937280.1:n.601-168_601-167insCACCTTCAGGTAAATGGGCTCATCCTTTGAGCCATGAGGATGGGAAGCGAAGCAAGGAATGAAAAAGCTAG
XM_017027680.1:c.878-8844_878-8843insCTAGCTTTTTCATTCCTTGCTTCGCTTCCCATCCTCATGGCTCAAAGGATGAGCCCATTTACCTGAAGGTG (ISM1) XP_016883169.1:n.878-8844_878-8843insCTAGCTTTTTCATTCCTTGCTTCG...
XR_001754319.2:n.1282-168_1282-167insCACCTTCAGGTAAATGGGCTCATCCTTTGAGCCATGAGGATGGGAAGCGAAGCAAGGAATGAAAAAGCTAG (TASP1)