Canonical Allele Identifier: CA2012557328

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109125_3109127delinsCGG , CM000674.2:g.3109125_3109127delinsCGG	GRCh38
NC_000012.11:g.3218291_3218293delinsCGG , CM000674.1:g.3218291_3218293delinsCGG	GRCh37
NC_000012.10:g.3088552_3088554delinsCGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25406_-18+25408delinsCGG MANE Select	ENSP00000011898.5:n.-18+25406_-18+25408delinsCGG
ENST00000649909.1:c.-130+25406_-130+25408delinsCGG	ENSP00000497370.1:n.-130+25406_-130+25408delinsCGG
ENST00000011898.9:c.-18+25406_-18+25408delinsCGG	ENSP00000011898.5:n.-18+25406_-18+25408delinsCGG
ENST00000444315.6:c.-18+25406_-18+25408delinsCGG	ENSP00000412908.2:n.-18+25406_-18+25408delinsCGG
ENST00000537971.5:c.-18+31672_-18+31674delinsCGG	ENSP00000444799.1:n.-18+31672_-18+31674delinsCGG
NM_001168320.1:c.-18+31672_-18+31674delinsCGG	NP_001161792.1:n.-18+31672_-18+31674delinsCGG
NM_006675.4:c.-18+25406_-18+25408delinsCGG	NP_006666.1:n.-18+25406_-18+25408delinsCGG
XM_011520912.1:c.-349+25406_-349+25408delinsCGG	XP_011519214.1:n.-349+25406_-349+25408delinsCGG
XM_011520912.3:c.-349+25406_-349+25408delinsCGG	XP_011519214.1:n.-349+25406_-349+25408delinsCGG
NM_006675.5:c.-18+25406_-18+25408delinsCGG MANE Select	NP_006666.1:n.-18+25406_-18+25408delinsCGG
NM_001168320.2:c.-18+31672_-18+31674delinsCGG	NP_001161792.1:n.-18+31672_-18+31674delinsCGG