Canonical Allele Identifier: CA687272731
Gene: TSPAN9 HGNC NCBI

Linked Data

dbSNP Id: rs1392219043

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3109298_3109299insAGAGAG , CM000674.2:g.3109298_3109299insAGAGAG GRCh38
NC_000012.11:g.3218464_3218465insAGAGAG , CM000674.1:g.3218464_3218465insAGAGAG GRCh37
NC_000012.10:g.3088725_3088726insAGAGAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000011898.10:c.-18+25579_-18+25580insAGAGAG MANE Select ENSP00000011898.5:n.-18+25579_-18+25580insAGAGAG
ENST00000649909.1:c.-130+25579_-130+25580insAGAGAG ENSP00000497370.1:n.-130+25579_-130+25580insAGAGAG
ENST00000011898.9:c.-18+25579_-18+25580insAGAGAG ENSP00000011898.5:n.-18+25579_-18+25580insAGAGAG
ENST00000444315.6:c.-18+25579_-18+25580insAGAGAG ENSP00000412908.2:n.-18+25579_-18+25580insAGAGAG
ENST00000537971.5:c.-18+31845_-18+31846insAGAGAG ENSP00000444799.1:n.-18+31845_-18+31846insAGAGAG
NM_001168320.1:c.-18+31845_-18+31846insAGAGAG NP_001161792.1:n.-18+31845_-18+31846insAGAGAG
NM_006675.4:c.-18+25579_-18+25580insAGAGAG NP_006666.1:n.-18+25579_-18+25580insAGAGAG
XM_011520912.1:c.-349+25579_-349+25580insAGAGAG XP_011519214.1:n.-349+25579_-349+25580insAGAGAG
XM_011520912.3:c.-349+25579_-349+25580insAGAGAG XP_011519214.1:n.-349+25579_-349+25580insAGAGAG
NM_006675.5:c.-18+25579_-18+25580insAGAGAG MANE Select NP_006666.1:n.-18+25579_-18+25580insAGAGAG
NM_001168320.2:c.-18+31845_-18+31846insAGAGAG NP_001161792.1:n.-18+31845_-18+31846insAGAGAG