Canonical Allele Identifier: CA2012557163

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108943_3108945delinsCTT , CM000674.2:g.3108943_3108945delinsCTT	GRCh38
NC_000012.11:g.3218109_3218111delinsCTT , CM000674.1:g.3218109_3218111delinsCTT	GRCh37
NC_000012.10:g.3088370_3088372delinsCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25224_-18+25226delinsCTT MANE Select	ENSP00000011898.5:n.-18+25224_-18+25226delinsCTT
ENST00000649909.1:c.-130+25224_-130+25226delinsCTT	ENSP00000497370.1:n.-130+25224_-130+25226delinsCTT
ENST00000011898.9:c.-18+25224_-18+25226delinsCTT	ENSP00000011898.5:n.-18+25224_-18+25226delinsCTT
ENST00000444315.6:c.-18+25224_-18+25226delinsCTT	ENSP00000412908.2:n.-18+25224_-18+25226delinsCTT
ENST00000537971.5:c.-18+31490_-18+31492delinsCTT	ENSP00000444799.1:n.-18+31490_-18+31492delinsCTT
NM_001168320.1:c.-18+31490_-18+31492delinsCTT	NP_001161792.1:n.-18+31490_-18+31492delinsCTT
NM_006675.4:c.-18+25224_-18+25226delinsCTT	NP_006666.1:n.-18+25224_-18+25226delinsCTT
XM_011520912.1:c.-349+25224_-349+25226delinsCTT	XP_011519214.1:n.-349+25224_-349+25226delinsCTT
XM_011520912.3:c.-349+25224_-349+25226delinsCTT	XP_011519214.1:n.-349+25224_-349+25226delinsCTT
NM_006675.5:c.-18+25224_-18+25226delinsCTT MANE Select	NP_006666.1:n.-18+25224_-18+25226delinsCTT
NM_001168320.2:c.-18+31490_-18+31492delinsCTT	NP_001161792.1:n.-18+31490_-18+31492delinsCTT