Canonical Allele Identifier: CA2012557508

Gene: TSPAN9

Linked Data

• dbSNP Id: rs2098316804

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109289_3109290insATGTGT , CM000674.2:g.3109289_3109290insATGTGT	GRCh38
NC_000012.11:g.3218455_3218456insATGTGT , CM000674.1:g.3218455_3218456insATGTGT	GRCh37
NC_000012.10:g.3088716_3088717insATGTGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25570_-18+25571insATGTGT MANE Select	ENSP00000011898.5:n.-18+25570_-18+25571insATGTGT
ENST00000649909.1:c.-130+25570_-130+25571insATGTGT	ENSP00000497370.1:n.-130+25570_-130+25571insATGTGT
ENST00000011898.9:c.-18+25570_-18+25571insATGTGT	ENSP00000011898.5:n.-18+25570_-18+25571insATGTGT
ENST00000444315.6:c.-18+25570_-18+25571insATGTGT	ENSP00000412908.2:n.-18+25570_-18+25571insATGTGT
ENST00000537971.5:c.-18+31836_-18+31837insATGTGT	ENSP00000444799.1:n.-18+31836_-18+31837insATGTGT
NM_001168320.1:c.-18+31836_-18+31837insATGTGT	NP_001161792.1:n.-18+31836_-18+31837insATGTGT
NM_006675.4:c.-18+25570_-18+25571insATGTGT	NP_006666.1:n.-18+25570_-18+25571insATGTGT
XM_011520912.1:c.-349+25570_-349+25571insATGTGT	XP_011519214.1:n.-349+25570_-349+25571insATGTGT
XM_011520912.3:c.-349+25570_-349+25571insATGTGT	XP_011519214.1:n.-349+25570_-349+25571insATGTGT
NM_006675.5:c.-18+25570_-18+25571insATGTGT MANE Select	NP_006666.1:n.-18+25570_-18+25571insATGTGT
NM_001168320.2:c.-18+31836_-18+31837insATGTGT	NP_001161792.1:n.-18+31836_-18+31837insATGTGT