Canonical Allele Identifier: CA2012557213
Gene: TSPAN9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3109010A= , CM000674.2:g.3109010A= GRCh38
NC_000012.11:g.3218176A= , CM000674.1:g.3218176A= GRCh37
NC_000012.10:g.3088437A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000011898.10:c.-18+25291A= MANE Select ENSP00000011898.5:n.-18+25291A=
ENST00000649909.1:c.-130+25291A= ENSP00000497370.1:n.-130+25291A=
ENST00000011898.9:c.-18+25291A= ENSP00000011898.5:n.-18+25291A=
ENST00000444315.6:c.-18+25291A= ENSP00000412908.2:n.-18+25291A=
ENST00000537971.5:c.-18+31557A= ENSP00000444799.1:n.-18+31557A=
NM_001168320.1:c.-18+31557A= NP_001161792.1:n.-18+31557A=
NM_006675.4:c.-18+25291A= NP_006666.1:n.-18+25291A=
XM_011520912.1:c.-349+25291A= XP_011519214.1:n.-349+25291A=
XM_011520912.3:c.-349+25291A= XP_011519214.1:n.-349+25291A=
NM_006675.5:c.-18+25291A= MANE Select NP_006666.1:n.-18+25291A=
NM_001168320.2:c.-18+31557A= NP_001161792.1:n.-18+31557A=
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