Canonical Allele Identifier: CA944146357

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1555141856
• gnomAD v3: 12-3109268-C-CTGTCTGTGTGTG
• gnomAD v4: 12-3109268-C-CTGTCTGTGTGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109271_3109272insCTGTGTGTGTGT , CM000674.2:g.3109271_3109272insCTGTGTGTGTGT	GRCh38
NC_000012.11:g.3218437_3218438insCTGTGTGTGTGT , CM000674.1:g.3218437_3218438insCTGTGTGTGTGT	GRCh37
NC_000012.10:g.3088698_3088699insCTGTGTGTGTGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25552_-18+25553insCTGTGTGTGTGT MANE Select	ENSP00000011898.5:n.-18+25552_-18+25553insCTGTGTGTGTGT
ENST00000649909.1:c.-130+25552_-130+25553insCTGTGTGTGTGT	ENSP00000497370.1:n.-130+25552_-130+25553insCTGTGTGTGTGT
ENST00000011898.9:c.-18+25552_-18+25553insCTGTGTGTGTGT	ENSP00000011898.5:n.-18+25552_-18+25553insCTGTGTGTGTGT
ENST00000444315.6:c.-18+25552_-18+25553insCTGTGTGTGTGT	ENSP00000412908.2:n.-18+25552_-18+25553insCTGTGTGTGTGT
ENST00000537971.5:c.-18+31818_-18+31819insCTGTGTGTGTGT	ENSP00000444799.1:n.-18+31818_-18+31819insCTGTGTGTGTGT
NM_001168320.1:c.-18+31818_-18+31819insCTGTGTGTGTGT	NP_001161792.1:n.-18+31818_-18+31819insCTGTGTGTGTGT
NM_006675.4:c.-18+25552_-18+25553insCTGTGTGTGTGT	NP_006666.1:n.-18+25552_-18+25553insCTGTGTGTGTGT
XM_011520912.1:c.-349+25552_-349+25553insCTGTGTGTGTGT	XP_011519214.1:n.-349+25552_-349+25553insCTGTGTGTGTGT
XM_011520912.3:c.-349+25552_-349+25553insCTGTGTGTGTGT	XP_011519214.1:n.-349+25552_-349+25553insCTGTGTGTGTGT
NM_006675.5:c.-18+25552_-18+25553insCTGTGTGTGTGT MANE Select	NP_006666.1:n.-18+25552_-18+25553insCTGTGTGTGTGT
NM_001168320.2:c.-18+31818_-18+31819insCTGTGTGTGTGT	NP_001161792.1:n.-18+31818_-18+31819insCTGTGTGTGTGT