Canonical Allele Identifier: CA944146244
Gene: TSPAN9 HGNC NCBI

Linked Data

dbSNP Id: rs1461795540

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3109267_3109268insGTGTGTGTGTGT , CM000674.2:g.3109267_3109268insGTGTGTGTGTGT GRCh38
NC_000012.11:g.3218433_3218434insGTGTGTGTGTGT , CM000674.1:g.3218433_3218434insGTGTGTGTGTGT GRCh37
NC_000012.10:g.3088694_3088695insGTGTGTGTGTGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000011898.10:c.-18+25548_-18+25549insGTGTGTGTGTGT MANE Select ENSP00000011898.5:n.-18+25548_-18+25549insGTGTGTGTGTGT
ENST00000649909.1:c.-130+25548_-130+25549insGTGTGTGTGTGT ENSP00000497370.1:n.-130+25548_-130+25549insGTGTGTGTGTGT
ENST00000011898.9:c.-18+25548_-18+25549insGTGTGTGTGTGT ENSP00000011898.5:n.-18+25548_-18+25549insGTGTGTGTGTGT
ENST00000444315.6:c.-18+25548_-18+25549insGTGTGTGTGTGT ENSP00000412908.2:n.-18+25548_-18+25549insGTGTGTGTGTGT
ENST00000537971.5:c.-18+31814_-18+31815insGTGTGTGTGTGT ENSP00000444799.1:n.-18+31814_-18+31815insGTGTGTGTGTGT
NM_001168320.1:c.-18+31814_-18+31815insGTGTGTGTGTGT NP_001161792.1:n.-18+31814_-18+31815insGTGTGTGTGTGT
NM_006675.4:c.-18+25548_-18+25549insGTGTGTGTGTGT NP_006666.1:n.-18+25548_-18+25549insGTGTGTGTGTGT
XM_011520912.1:c.-349+25548_-349+25549insGTGTGTGTGTGT XP_011519214.1:n.-349+25548_-349+25549insGTGTGTGTGTGT
XM_011520912.3:c.-349+25548_-349+25549insGTGTGTGTGTGT XP_011519214.1:n.-349+25548_-349+25549insGTGTGTGTGTGT
NM_006675.5:c.-18+25548_-18+25549insGTGTGTGTGTGT MANE Select NP_006666.1:n.-18+25548_-18+25549insGTGTGTGTGTGT
NM_001168320.2:c.-18+31814_-18+31815insGTGTGTGTGTGT NP_001161792.1:n.-18+31814_-18+31815insGTGTGTGTGTGT