Canonical Allele Identifier: CA687272964

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1274383200
• gnomAD v3: 12-3109299-T-TGTGAGAGAGAGAGAGA
• gnomAD v4: 12-3109299-T-TGTGAGAGAGAGAGAGA
• MyVariant Identifiers: chr12:g.3218465_3218466insGTGAGAGAGAGAGAGA (hg19) ; chr12:g.3109299_3109300insGTGAGAGAGAGAGAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109300_3109301insTGAGAGAGAGAGAGAG , CM000674.2:g.3109300_3109301insTGAGAGAGAGAGAGAG	GRCh38
NC_000012.11:g.3218466_3218467insTGAGAGAGAGAGAGAG , CM000674.1:g.3218466_3218467insTGAGAGAGAGAGAGAG	GRCh37
NC_000012.10:g.3088727_3088728insTGAGAGAGAGAGAGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25581_-18+25582insTGAGAGAGAGAGAGAG MANE Select	ENSP00000011898.5:n.-18+25581_-18+25582insTGAGAGAGAGAGAGAG
ENST00000649909.1:c.-130+25581_-130+25582insTGAGAGAGAGAGAGAG	ENSP00000497370.1:n.-130+25581_-130+25582insTGAGAGAGAGAGAGAG
ENST00000011898.9:c.-18+25581_-18+25582insTGAGAGAGAGAGAGAG	ENSP00000011898.5:n.-18+25581_-18+25582insTGAGAGAGAGAGAGAG
ENST00000444315.6:c.-18+25581_-18+25582insTGAGAGAGAGAGAGAG	ENSP00000412908.2:n.-18+25581_-18+25582insTGAGAGAGAGAGAGAG
ENST00000537971.5:c.-18+31847_-18+31848insTGAGAGAGAGAGAGAG	ENSP00000444799.1:n.-18+31847_-18+31848insTGAGAGAGAGAGAGAG
NM_001168320.1:c.-18+31847_-18+31848insTGAGAGAGAGAGAGAG	NP_001161792.1:n.-18+31847_-18+31848insTGAGAGAGAGAGAGAG
NM_006675.4:c.-18+25581_-18+25582insTGAGAGAGAGAGAGAG	NP_006666.1:n.-18+25581_-18+25582insTGAGAGAGAGAGAGAG
XM_011520912.1:c.-349+25581_-349+25582insTGAGAGAGAGAGAGAG	XP_011519214.1:n.-349+25581_-349+25582insTGAGAGAGAGAGAGAG
XM_011520912.3:c.-349+25581_-349+25582insTGAGAGAGAGAGAGAG	XP_011519214.1:n.-349+25581_-349+25582insTGAGAGAGAGAGAGAG
NM_006675.5:c.-18+25581_-18+25582insTGAGAGAGAGAGAGAG MANE Select	NP_006666.1:n.-18+25581_-18+25582insTGAGAGAGAGAGAGAG
NM_001168320.2:c.-18+31847_-18+31848insTGAGAGAGAGAGAGAG	NP_001161792.1:n.-18+31847_-18+31848insTGAGAGAGAGAGAGAG