Canonical Allele Identifier: CA2794333012

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108956_3108959del , CM000674.2:g.3108956_3108959del	GRCh38
NC_000012.11:g.3218122_3218125del , CM000674.1:g.3218122_3218125del	GRCh37
NC_000012.10:g.3088383_3088386del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25237_-18+25240del MANE Select	ENSP00000011898.5:n.-18+25237_-18+25240del
ENST00000649909.1:c.-130+25237_-130+25240del	ENSP00000497370.1:n.-130+25237_-130+25240del
ENST00000011898.9:c.-18+25237_-18+25240del	ENSP00000011898.5:n.-18+25237_-18+25240del
ENST00000444315.6:c.-18+25237_-18+25240del	ENSP00000412908.2:n.-18+25237_-18+25240del
ENST00000537971.5:c.-18+31503_-18+31506del	ENSP00000444799.1:n.-18+31503_-18+31506del
NM_001168320.1:c.-18+31503_-18+31506del	NP_001161792.1:n.-18+31503_-18+31506del
NM_006675.4:c.-18+25237_-18+25240del	NP_006666.1:n.-18+25237_-18+25240del
XM_011520912.1:c.-349+25237_-349+25240del	XP_011519214.1:n.-349+25237_-349+25240del
XM_011520912.3:c.-349+25237_-349+25240del	XP_011519214.1:n.-349+25237_-349+25240del
NM_006675.5:c.-18+25237_-18+25240del MANE Select	NP_006666.1:n.-18+25237_-18+25240del
NM_001168320.2:c.-18+31503_-18+31506del	NP_001161792.1:n.-18+31503_-18+31506del