Canonical Allele Identifier: CA2012557180

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108972_3108973delinsCT , CM000674.2:g.3108972_3108973delinsCT	GRCh38
NC_000012.11:g.3218138_3218139delinsCT , CM000674.1:g.3218138_3218139delinsCT	GRCh37
NC_000012.10:g.3088399_3088400delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25253_-18+25254delinsCT MANE Select	ENSP00000011898.5:n.-18+25253_-18+25254delinsCT
ENST00000649909.1:c.-130+25253_-130+25254delinsCT	ENSP00000497370.1:n.-130+25253_-130+25254delinsCT
ENST00000011898.9:c.-18+25253_-18+25254delinsCT	ENSP00000011898.5:n.-18+25253_-18+25254delinsCT
ENST00000444315.6:c.-18+25253_-18+25254delinsCT	ENSP00000412908.2:n.-18+25253_-18+25254delinsCT
ENST00000537971.5:c.-18+31519_-18+31520delinsCT	ENSP00000444799.1:n.-18+31519_-18+31520delinsCT
NM_001168320.1:c.-18+31519_-18+31520delinsCT	NP_001161792.1:n.-18+31519_-18+31520delinsCT
NM_006675.4:c.-18+25253_-18+25254delinsCT	NP_006666.1:n.-18+25253_-18+25254delinsCT
XM_011520912.1:c.-349+25253_-349+25254delinsCT	XP_011519214.1:n.-349+25253_-349+25254delinsCT
XM_011520912.3:c.-349+25253_-349+25254delinsCT	XP_011519214.1:n.-349+25253_-349+25254delinsCT
NM_006675.5:c.-18+25253_-18+25254delinsCT MANE Select	NP_006666.1:n.-18+25253_-18+25254delinsCT
NM_001168320.2:c.-18+31519_-18+31520delinsCT	NP_001161792.1:n.-18+31519_-18+31520delinsCT