Canonical Allele Identifier: CA2012557483
Gene: TSPAN9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3109268_3109284delinsCTGTGTGTGTGTGTGTG , CM000674.2:g.3109268_3109284delinsCTGTGTGTGTGTGTGTG GRCh38
NC_000012.11:g.3218434_3218450delinsCTGTGTGTGTGTGTGTG , CM000674.1:g.3218434_3218450delinsCTGTGTGTGTGTGTGTG GRCh37
NC_000012.10:g.3088695_3088711delinsCTGTGTGTGTGTGTGTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000011898.10:c.-18+25549_-18+25565delinsCTGTGTGTGTGTGTGTG MANE Select ENSP00000011898.5:n.-18+25549_-18+25565delinsCTGTGTGTGTGTGTGT...
ENST00000649909.1:c.-130+25549_-130+25565delinsCTGTGTGTGTGTGTGTG ENSP00000497370.1:n.-130+25549_-130+25565delinsCTGTGTGTGTGTGT...
ENST00000011898.9:c.-18+25549_-18+25565delinsCTGTGTGTGTGTGTGTG ENSP00000011898.5:n.-18+25549_-18+25565delinsCTGTGTGTGTGTGTGT...
ENST00000444315.6:c.-18+25549_-18+25565delinsCTGTGTGTGTGTGTGTG ENSP00000412908.2:n.-18+25549_-18+25565delinsCTGTGTGTGTGTGTGT...
ENST00000537971.5:c.-18+31815_-18+31831delinsCTGTGTGTGTGTGTGTG ENSP00000444799.1:n.-18+31815_-18+31831delinsCTGTGTGTGTGTGTGT...
NM_001168320.1:c.-18+31815_-18+31831delinsCTGTGTGTGTGTGTGTG NP_001161792.1:n.-18+31815_-18+31831delinsCTGTGTGTGTGTGTGTG
NM_006675.4:c.-18+25549_-18+25565delinsCTGTGTGTGTGTGTGTG NP_006666.1:n.-18+25549_-18+25565delinsCTGTGTGTGTGTGTGTG
XM_011520912.1:c.-349+25549_-349+25565delinsCTGTGTGTGTGTGTGTG XP_011519214.1:n.-349+25549_-349+25565delinsCTGTGTGTGTGTGTGTG...
XM_011520912.3:c.-349+25549_-349+25565delinsCTGTGTGTGTGTGTGTG XP_011519214.1:n.-349+25549_-349+25565delinsCTGTGTGTGTGTGTGTG...
NM_006675.5:c.-18+25549_-18+25565delinsCTGTGTGTGTGTGTGTG MANE Select NP_006666.1:n.-18+25549_-18+25565delinsCTGTGTGTGTGTGTGTG
NM_001168320.2:c.-18+31815_-18+31831delinsCTGTGTGTGTGTGTGTG NP_001161792.1:n.-18+31815_-18+31831delinsCTGTGTGTGTGTGTGTG