Canonical Allele Identifier: CA2012557530

Gene: TSPAN9

Linked Data

• dbSNP Id: rs2098316858

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109298_3109299insAGAGTGTG , CM000674.2:g.3109298_3109299insAGAGTGTG	GRCh38
NC_000012.11:g.3218464_3218465insAGAGTGTG , CM000674.1:g.3218464_3218465insAGAGTGTG	GRCh37
NC_000012.10:g.3088725_3088726insAGAGTGTG	NCBI36

Transcript Alleles

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