Canonical Allele Identifier: CA2012557226

Gene: TSPAN9

Linked Data

• dbSNP Id: rs2098316239

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109023_3109024dup , CM000674.2:g.3109023_3109024dup	GRCh38
NC_000012.11:g.3218189_3218190dup , CM000674.1:g.3218189_3218190dup	GRCh37
NC_000012.10:g.3088450_3088451dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25304_-18+25305dup MANE Select	ENSP00000011898.5:n.-18+25304_-18+25305dup
ENST00000649909.1:c.-130+25304_-130+25305dup	ENSP00000497370.1:n.-130+25304_-130+25305dup
ENST00000011898.9:c.-18+25304_-18+25305dup	ENSP00000011898.5:n.-18+25304_-18+25305dup
ENST00000444315.6:c.-18+25304_-18+25305dup	ENSP00000412908.2:n.-18+25304_-18+25305dup
ENST00000537971.5:c.-18+31570_-18+31571dup	ENSP00000444799.1:n.-18+31570_-18+31571dup
NM_001168320.1:c.-18+31570_-18+31571dup	NP_001161792.1:n.-18+31570_-18+31571dup
NM_006675.4:c.-18+25304_-18+25305dup	NP_006666.1:n.-18+25304_-18+25305dup
XM_011520912.1:c.-349+25304_-349+25305dup	XP_011519214.1:n.-349+25304_-349+25305dup
XM_011520912.3:c.-349+25304_-349+25305dup	XP_011519214.1:n.-349+25304_-349+25305dup
NM_006675.5:c.-18+25304_-18+25305dup MANE Select	NP_006666.1:n.-18+25304_-18+25305dup
NM_001168320.2:c.-18+31570_-18+31571dup	NP_001161792.1:n.-18+31570_-18+31571dup