Canonical Allele Identifier: CA687273164

Gene: TSPAN9

Linked Data

• dbSNP Id: rs560687812
• gnomAD v3: 12-3109307-A-AGAGAGTGT
• gnomAD v4: 12-3109307-A-AGAGAGTGT
• MyVariant Identifiers: chr12:g.3218473_3218474insGAGAGTGT (hg19) ; chr12:g.3109307_3109308insGAGAGTGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109308_3109309insAGAGTGTG , CM000674.2:g.3109308_3109309insAGAGTGTG	GRCh38
NC_000012.11:g.3218474_3218475insAGAGTGTG , CM000674.1:g.3218474_3218475insAGAGTGTG	GRCh37
NC_000012.10:g.3088735_3088736insAGAGTGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25589_-18+25590insAGAGTGTG MANE Select	ENSP00000011898.5:n.-18+25589_-18+25590insAGAGTGTG
ENST00000649909.1:c.-130+25589_-130+25590insAGAGTGTG	ENSP00000497370.1:n.-130+25589_-130+25590insAGAGTGTG
ENST00000011898.9:c.-18+25589_-18+25590insAGAGTGTG	ENSP00000011898.5:n.-18+25589_-18+25590insAGAGTGTG
ENST00000444315.6:c.-18+25589_-18+25590insAGAGTGTG	ENSP00000412908.2:n.-18+25589_-18+25590insAGAGTGTG
ENST00000537971.5:c.-18+31855_-18+31856insAGAGTGTG	ENSP00000444799.1:n.-18+31855_-18+31856insAGAGTGTG
NM_001168320.1:c.-18+31855_-18+31856insAGAGTGTG	NP_001161792.1:n.-18+31855_-18+31856insAGAGTGTG
NM_006675.4:c.-18+25589_-18+25590insAGAGTGTG	NP_006666.1:n.-18+25589_-18+25590insAGAGTGTG
XM_011520912.1:c.-349+25589_-349+25590insAGAGTGTG	XP_011519214.1:n.-349+25589_-349+25590insAGAGTGTG
XM_011520912.3:c.-349+25589_-349+25590insAGAGTGTG	XP_011519214.1:n.-349+25589_-349+25590insAGAGTGTG
NM_006675.5:c.-18+25589_-18+25590insAGAGTGTG MANE Select	NP_006666.1:n.-18+25589_-18+25590insAGAGTGTG
NM_001168320.2:c.-18+31855_-18+31856insAGAGTGTG	NP_001161792.1:n.-18+31855_-18+31856insAGAGTGTG