Canonical Allele Identifier: CA2725620544

Gene: TSPAN9

Linked Data

• dbSNP Id: rs2153965158

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109268_3109269del , CM000674.2:g.3109268_3109269del	GRCh38
NC_000012.11:g.3218434_3218435del , CM000674.1:g.3218434_3218435del	GRCh37
NC_000012.10:g.3088695_3088696del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25549_-18+25550del MANE Select	ENSP00000011898.5:n.-18+25549_-18+25550del
ENST00000649909.1:c.-130+25549_-130+25550del	ENSP00000497370.1:n.-130+25549_-130+25550del
ENST00000011898.9:c.-18+25549_-18+25550del	ENSP00000011898.5:n.-18+25549_-18+25550del
ENST00000444315.6:c.-18+25549_-18+25550del	ENSP00000412908.2:n.-18+25549_-18+25550del
ENST00000537971.5:c.-18+31815_-18+31816del	ENSP00000444799.1:n.-18+31815_-18+31816del
NM_001168320.1:c.-18+31815_-18+31816del	NP_001161792.1:n.-18+31815_-18+31816del
NM_006675.4:c.-18+25549_-18+25550del	NP_006666.1:n.-18+25549_-18+25550del
XM_011520912.1:c.-349+25549_-349+25550del	XP_011519214.1:n.-349+25549_-349+25550del
XM_011520912.3:c.-349+25549_-349+25550del	XP_011519214.1:n.-349+25549_-349+25550del
NM_006675.5:c.-18+25549_-18+25550del MANE Select	NP_006666.1:n.-18+25549_-18+25550del
NM_001168320.2:c.-18+31815_-18+31816del	NP_001161792.1:n.-18+31815_-18+31816del