Canonical Allele Identifier: CA944146414

Gene: TSPAN9

Linked Data

• dbSNP Id: rs2098316767
• gnomAD v3: 12-3109270-G-GTGTGTGTA
• gnomAD v4: 12-3109270-G-GTGTGTGTA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109277_3109278insATGTGTGT , CM000674.2:g.3109277_3109278insATGTGTGT	GRCh38
NC_000012.11:g.3218443_3218444insATGTGTGT , CM000674.1:g.3218443_3218444insATGTGTGT	GRCh37
NC_000012.10:g.3088704_3088705insATGTGTGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25558_-18+25559insATGTGTGT MANE Select	ENSP00000011898.5:n.-18+25558_-18+25559insATGTGTGT
ENST00000649909.1:c.-130+25558_-130+25559insATGTGTGT	ENSP00000497370.1:n.-130+25558_-130+25559insATGTGTGT
ENST00000011898.9:c.-18+25558_-18+25559insATGTGTGT	ENSP00000011898.5:n.-18+25558_-18+25559insATGTGTGT
ENST00000444315.6:c.-18+25558_-18+25559insATGTGTGT	ENSP00000412908.2:n.-18+25558_-18+25559insATGTGTGT
ENST00000537971.5:c.-18+31824_-18+31825insATGTGTGT	ENSP00000444799.1:n.-18+31824_-18+31825insATGTGTGT
NM_001168320.1:c.-18+31824_-18+31825insATGTGTGT	NP_001161792.1:n.-18+31824_-18+31825insATGTGTGT
NM_006675.4:c.-18+25558_-18+25559insATGTGTGT	NP_006666.1:n.-18+25558_-18+25559insATGTGTGT
XM_011520912.1:c.-349+25558_-349+25559insATGTGTGT	XP_011519214.1:n.-349+25558_-349+25559insATGTGTGT
XM_011520912.3:c.-349+25558_-349+25559insATGTGTGT	XP_011519214.1:n.-349+25558_-349+25559insATGTGTGT
NM_006675.5:c.-18+25558_-18+25559insATGTGTGT MANE Select	NP_006666.1:n.-18+25558_-18+25559insATGTGTGT
NM_001168320.2:c.-18+31824_-18+31825insATGTGTGT	NP_001161792.1:n.-18+31824_-18+31825insATGTGTGT