Canonical Allele Identifier: CA2012557320

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109122_3109123delinsAG , CM000674.2:g.3109122_3109123delinsAG	GRCh38
NC_000012.11:g.3218288_3218289delinsAG , CM000674.1:g.3218288_3218289delinsAG	GRCh37
NC_000012.10:g.3088549_3088550delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25403_-18+25404delinsAG MANE Select	ENSP00000011898.5:n.-18+25403_-18+25404delinsAG
ENST00000649909.1:c.-130+25403_-130+25404delinsAG	ENSP00000497370.1:n.-130+25403_-130+25404delinsAG
ENST00000011898.9:c.-18+25403_-18+25404delinsAG	ENSP00000011898.5:n.-18+25403_-18+25404delinsAG
ENST00000444315.6:c.-18+25403_-18+25404delinsAG	ENSP00000412908.2:n.-18+25403_-18+25404delinsAG
ENST00000537971.5:c.-18+31669_-18+31670delinsAG	ENSP00000444799.1:n.-18+31669_-18+31670delinsAG
NM_001168320.1:c.-18+31669_-18+31670delinsAG	NP_001161792.1:n.-18+31669_-18+31670delinsAG
NM_006675.4:c.-18+25403_-18+25404delinsAG	NP_006666.1:n.-18+25403_-18+25404delinsAG
XM_011520912.1:c.-349+25403_-349+25404delinsAG	XP_011519214.1:n.-349+25403_-349+25404delinsAG
XM_011520912.3:c.-349+25403_-349+25404delinsAG	XP_011519214.1:n.-349+25403_-349+25404delinsAG
NM_006675.5:c.-18+25403_-18+25404delinsAG MANE Select	NP_006666.1:n.-18+25403_-18+25404delinsAG
NM_001168320.2:c.-18+31669_-18+31670delinsAG	NP_001161792.1:n.-18+31669_-18+31670delinsAG