Canonical Allele Identifier: CA2012557595

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109324_3109325delinsGT , CM000674.2:g.3109324_3109325delinsGT	GRCh38
NC_000012.11:g.3218490_3218491delinsGT , CM000674.1:g.3218490_3218491delinsGT	GRCh37
NC_000012.10:g.3088751_3088752delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25605_-18+25606delinsGT MANE Select	ENSP00000011898.5:n.-18+25605_-18+25606delinsGT
ENST00000649909.1:c.-130+25605_-130+25606delinsGT	ENSP00000497370.1:n.-130+25605_-130+25606delinsGT
ENST00000011898.9:c.-18+25605_-18+25606delinsGT	ENSP00000011898.5:n.-18+25605_-18+25606delinsGT
ENST00000444315.6:c.-18+25605_-18+25606delinsGT	ENSP00000412908.2:n.-18+25605_-18+25606delinsGT
ENST00000537971.5:c.-18+31871_-18+31872delinsGT	ENSP00000444799.1:n.-18+31871_-18+31872delinsGT
NM_001168320.1:c.-18+31871_-18+31872delinsGT	NP_001161792.1:n.-18+31871_-18+31872delinsGT
NM_006675.4:c.-18+25605_-18+25606delinsGT	NP_006666.1:n.-18+25605_-18+25606delinsGT
XM_011520912.1:c.-349+25605_-349+25606delinsGT	XP_011519214.1:n.-349+25605_-349+25606delinsGT
XM_011520912.3:c.-349+25605_-349+25606delinsGT	XP_011519214.1:n.-349+25605_-349+25606delinsGT
NM_006675.5:c.-18+25605_-18+25606delinsGT MANE Select	NP_006666.1:n.-18+25605_-18+25606delinsGT
NM_001168320.2:c.-18+31871_-18+31872delinsGT	NP_001161792.1:n.-18+31871_-18+31872delinsGT