Canonical Allele Identifier: CA687271913

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1379341512
• gnomAD v3: 12-3108973-T-TG
• gnomAD v4: 12-3108973-T-TG
• MyVariant Identifiers: chr12:g.3218139_3218140insG (hg19) ; chr12:g.3108973_3108974insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108973_3108974insG , CM000674.2:g.3108973_3108974insG	GRCh38
NC_000012.11:g.3218139_3218140insG , CM000674.1:g.3218139_3218140insG	GRCh37
NC_000012.10:g.3088400_3088401insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25254_-18+25255insG MANE Select	ENSP00000011898.5:n.-18+25254_-18+25255insG
ENST00000649909.1:c.-130+25254_-130+25255insG	ENSP00000497370.1:n.-130+25254_-130+25255insG
ENST00000011898.9:c.-18+25254_-18+25255insG	ENSP00000011898.5:n.-18+25254_-18+25255insG
ENST00000444315.6:c.-18+25254_-18+25255insG	ENSP00000412908.2:n.-18+25254_-18+25255insG
ENST00000537971.5:c.-18+31520_-18+31521insG	ENSP00000444799.1:n.-18+31520_-18+31521insG
NM_001168320.1:c.-18+31520_-18+31521insG	NP_001161792.1:n.-18+31520_-18+31521insG
NM_006675.4:c.-18+25254_-18+25255insG	NP_006666.1:n.-18+25254_-18+25255insG
XM_011520912.1:c.-349+25254_-349+25255insG	XP_011519214.1:n.-349+25254_-349+25255insG
XM_011520912.3:c.-349+25254_-349+25255insG	XP_011519214.1:n.-349+25254_-349+25255insG
NM_006675.5:c.-18+25254_-18+25255insG MANE Select	NP_006666.1:n.-18+25254_-18+25255insG
NM_001168320.2:c.-18+31520_-18+31521insG	NP_001161792.1:n.-18+31520_-18+31521insG