Canonical Allele Identifier: CA2499398651

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109325_3109326insTT , CM000674.2:g.3109325_3109326insTT	GRCh38
NC_000012.11:g.3218491_3218492insTT , CM000674.1:g.3218491_3218492insTT	GRCh37
NC_000012.10:g.3088752_3088753insTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25606_-18+25607insTT MANE Select	ENSP00000011898.5:n.-18+25606_-18+25607insTT
ENST00000649909.1:c.-130+25606_-130+25607insTT	ENSP00000497370.1:n.-130+25606_-130+25607insTT
ENST00000011898.9:c.-18+25606_-18+25607insTT	ENSP00000011898.5:n.-18+25606_-18+25607insTT
ENST00000444315.6:c.-18+25606_-18+25607insTT	ENSP00000412908.2:n.-18+25606_-18+25607insTT
ENST00000537971.5:c.-18+31872_-18+31873insTT	ENSP00000444799.1:n.-18+31872_-18+31873insTT
NM_001168320.1:c.-18+31872_-18+31873insTT	NP_001161792.1:n.-18+31872_-18+31873insTT
NM_006675.4:c.-18+25606_-18+25607insTT	NP_006666.1:n.-18+25606_-18+25607insTT
XM_011520912.1:c.-349+25606_-349+25607insTT	XP_011519214.1:n.-349+25606_-349+25607insTT
XM_011520912.3:c.-349+25606_-349+25607insTT	XP_011519214.1:n.-349+25606_-349+25607insTT
NM_006675.5:c.-18+25606_-18+25607insTT MANE Select	NP_006666.1:n.-18+25606_-18+25607insTT
NM_001168320.2:c.-18+31872_-18+31873insTT	NP_001161792.1:n.-18+31872_-18+31873insTT