Canonical Allele Identifier: CA687272516

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1461795540
• gnomAD v3: 12-3109265-A-AGTGT
• gnomAD v4: 12-3109265-A-AGTGT
• MyVariant Identifiers: chr12:g.3218431_3218432insGTGT (hg19) ; chr12:g.3109265_3109266insGTGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109267_3109268insGTGT , CM000674.2:g.3109267_3109268insGTGT	GRCh38
NC_000012.11:g.3218433_3218434insGTGT , CM000674.1:g.3218433_3218434insGTGT	GRCh37
NC_000012.10:g.3088694_3088695insGTGT	NCBI36

Transcript Alleles

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