Canonical Allele Identifier: CA2012557307

Gene: TSPAN9

Linked Data

• dbSNP Id: rs536696660

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109107_3109108del , CM000674.2:g.3109107_3109108del	GRCh38
NC_000012.11:g.3218273_3218274del , CM000674.1:g.3218273_3218274del	GRCh37
NC_000012.10:g.3088534_3088535del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25388_-18+25389del MANE Select	ENSP00000011898.5:n.-18+25388_-18+25389del
ENST00000649909.1:c.-130+25388_-130+25389del	ENSP00000497370.1:n.-130+25388_-130+25389del
ENST00000011898.9:c.-18+25388_-18+25389del	ENSP00000011898.5:n.-18+25388_-18+25389del
ENST00000444315.6:c.-18+25388_-18+25389del	ENSP00000412908.2:n.-18+25388_-18+25389del
ENST00000537971.5:c.-18+31654_-18+31655del	ENSP00000444799.1:n.-18+31654_-18+31655del
NM_001168320.1:c.-18+31654_-18+31655del	NP_001161792.1:n.-18+31654_-18+31655del
NM_006675.4:c.-18+25388_-18+25389del	NP_006666.1:n.-18+25388_-18+25389del
XM_011520912.1:c.-349+25388_-349+25389del	XP_011519214.1:n.-349+25388_-349+25389del
XM_011520912.3:c.-349+25388_-349+25389del	XP_011519214.1:n.-349+25388_-349+25389del
NM_006675.5:c.-18+25388_-18+25389del MANE Select	NP_006666.1:n.-18+25388_-18+25389del
NM_001168320.2:c.-18+31654_-18+31655del	NP_001161792.1:n.-18+31654_-18+31655del