Canonical Allele Identifier: CA687272339

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1372052975
• gnomAD v3: 12-3109168-C-CCT
• gnomAD v4: 12-3109168-C-CCT
• MyVariant Identifiers: chr12:g.3218334_3218335insCT (hg19) ; chr12:g.3109168_3109169insCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109170_3109171dup , CM000674.2:g.3109170_3109171dup	GRCh38
NC_000012.11:g.3218336_3218337dup , CM000674.1:g.3218336_3218337dup	GRCh37
NC_000012.10:g.3088597_3088598dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25451_-18+25452dup MANE Select	ENSP00000011898.5:n.-18+25451_-18+25452dup
ENST00000649909.1:c.-130+25451_-130+25452dup	ENSP00000497370.1:n.-130+25451_-130+25452dup
ENST00000011898.9:c.-18+25451_-18+25452dup	ENSP00000011898.5:n.-18+25451_-18+25452dup
ENST00000444315.6:c.-18+25451_-18+25452dup	ENSP00000412908.2:n.-18+25451_-18+25452dup
ENST00000537971.5:c.-18+31717_-18+31718dup	ENSP00000444799.1:n.-18+31717_-18+31718dup
NM_001168320.1:c.-18+31717_-18+31718dup	NP_001161792.1:n.-18+31717_-18+31718dup
NM_006675.4:c.-18+25451_-18+25452dup	NP_006666.1:n.-18+25451_-18+25452dup
XM_011520912.1:c.-349+25451_-349+25452dup	XP_011519214.1:n.-349+25451_-349+25452dup
XM_011520912.3:c.-349+25451_-349+25452dup	XP_011519214.1:n.-349+25451_-349+25452dup
NM_006675.5:c.-18+25451_-18+25452dup MANE Select	NP_006666.1:n.-18+25451_-18+25452dup
NM_001168320.2:c.-18+31717_-18+31718dup	NP_001161792.1:n.-18+31717_-18+31718dup