Canonical Allele Identifier: CA2794333019
Gene: TSPAN9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3109129_3109130insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG , CM000674.2:g.3109129_3109130insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG GRCh38
NC_000012.11:g.3218295_3218296insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG , CM000674.1:g.3218295_3218296insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG GRCh37
NC_000012.10:g.3088556_3088557insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000011898.10:c.-18+25410_-18+25411insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG MANE Select ENSP00000011898.5:n.-18+25410_-18+25411insTTTCACCGTGTTAGCCAGG...
ENST00000649909.1:c.-130+25410_-130+25411insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG ENSP00000497370.1:n.-130+25410_-130+25411insTTTCACCGTGTTAGCCA...
ENST00000011898.9:c.-18+25410_-18+25411insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG ENSP00000011898.5:n.-18+25410_-18+25411insTTTCACCGTGTTAGCCAGG...
ENST00000444315.6:c.-18+25410_-18+25411insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG ENSP00000412908.2:n.-18+25410_-18+25411insTTTCACCGTGTTAGCCAGG...
ENST00000537971.5:c.-18+31676_-18+31677insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG ENSP00000444799.1:n.-18+31676_-18+31677insTTTCACCGTGTTAGCCAGG...
NM_001168320.1:c.-18+31676_-18+31677insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG NP_001161792.1:n.-18+31676_-18+31677insTTTCACCGTGTTAGCCAGGATG...
NM_006675.4:c.-18+25410_-18+25411insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG NP_006666.1:n.-18+25410_-18+25411insTTTCACCGTGTTAGCCAGGATGGTC...
XM_011520912.1:c.-349+25410_-349+25411insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG XP_011519214.1:n.-349+25410_-349+25411insTTTCACCGTGTTAGCCAGGA...
XM_011520912.3:c.-349+25410_-349+25411insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG XP_011519214.1:n.-349+25410_-349+25411insTTTCACCGTGTTAGCCAGGA...
NM_006675.5:c.-18+25410_-18+25411insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG MANE Select NP_006666.1:n.-18+25410_-18+25411insTTTCACCGTGTTAGCCAGGATGGTC...
NM_001168320.2:c.-18+31676_-18+31677insTTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGCACTCGCCACCACGCCCGGCTAATTTTTTGCATTTTTAGTAGAGACGGGG NP_001161792.1:n.-18+31676_-18+31677insTTTCACCGTGTTAGCCAGGATG...