Canonical Allele Identifier: CA919008782

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1565578731

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109081_3109083delinsGCG , CM000674.2:g.3109081_3109083delinsGCG	GRCh38
NC_000012.11:g.3218247_3218249delinsGCG , CM000674.1:g.3218247_3218249delinsGCG	GRCh37
NC_000012.10:g.3088508_3088510delinsGCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25362_-18+25364delinsGCG MANE Select	ENSP00000011898.5:n.-18+25362_-18+25364delinsGCG
ENST00000649909.1:c.-130+25362_-130+25364delinsGCG	ENSP00000497370.1:n.-130+25362_-130+25364delinsGCG
ENST00000011898.9:c.-18+25362_-18+25364delinsGCG	ENSP00000011898.5:n.-18+25362_-18+25364delinsGCG
ENST00000444315.6:c.-18+25362_-18+25364delinsGCG	ENSP00000412908.2:n.-18+25362_-18+25364delinsGCG
ENST00000537971.5:c.-18+31628_-18+31630delinsGCG	ENSP00000444799.1:n.-18+31628_-18+31630delinsGCG
NM_001168320.1:c.-18+31628_-18+31630delinsGCG	NP_001161792.1:n.-18+31628_-18+31630delinsGCG
NM_006675.4:c.-18+25362_-18+25364delinsGCG	NP_006666.1:n.-18+25362_-18+25364delinsGCG
XM_011520912.1:c.-349+25362_-349+25364delinsGCG	XP_011519214.1:n.-349+25362_-349+25364delinsGCG
XM_011520912.3:c.-349+25362_-349+25364delinsGCG	XP_011519214.1:n.-349+25362_-349+25364delinsGCG
NM_006675.5:c.-18+25362_-18+25364delinsGCG MANE Select	NP_006666.1:n.-18+25362_-18+25364delinsGCG
NM_001168320.2:c.-18+31628_-18+31630delinsGCG	NP_001161792.1:n.-18+31628_-18+31630delinsGCG