Canonical Allele Identifier: CA2590666426

Gene: TSPAN9

Linked Data

• gnomAD v3: 12-3109323-T-TAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA
• gnomAD v4: 12-3109323-T-TAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109323_3109324insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA , CM000674.2:g.3109323_3109324insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	GRCh38
NC_000012.11:g.3218489_3218490insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA , CM000674.1:g.3218489_3218490insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	GRCh37
NC_000012.10:g.3088750_3088751insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25604_-18+25605insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA MANE Select	ENSP00000011898.5:n.-18+25604_-18+25605insAAGAGAGAGAGATCTAATT...
ENST00000649909.1:c.-130+25604_-130+25605insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	ENSP00000497370.1:n.-130+25604_-130+25605insAAGAGAGAGAGATCTAA...
ENST00000011898.9:c.-18+25604_-18+25605insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	ENSP00000011898.5:n.-18+25604_-18+25605insAAGAGAGAGAGATCTAATT...
ENST00000444315.6:c.-18+25604_-18+25605insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	ENSP00000412908.2:n.-18+25604_-18+25605insAAGAGAGAGAGATCTAATT...
ENST00000537971.5:c.-18+31870_-18+31871insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	ENSP00000444799.1:n.-18+31870_-18+31871insAAGAGAGAGAGATCTAATT...
NM_001168320.1:c.-18+31870_-18+31871insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	NP_001161792.1:n.-18+31870_-18+31871insAAGAGAGAGAGATCTAATTTTT...
NM_006675.4:c.-18+25604_-18+25605insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	NP_006666.1:n.-18+25604_-18+25605insAAGAGAGAGAGATCTAATTTTTACA...
XM_011520912.1:c.-349+25604_-349+25605insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	XP_011519214.1:n.-349+25604_-349+25605insAAGAGAGAGAGATCTAATTT...
XM_011520912.3:c.-349+25604_-349+25605insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	XP_011519214.1:n.-349+25604_-349+25605insAAGAGAGAGAGATCTAATTT...
NM_006675.5:c.-18+25604_-18+25605insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA MANE Select	NP_006666.1:n.-18+25604_-18+25605insAAGAGAGAGAGATCTAATTTTTACA...
NM_001168320.2:c.-18+31870_-18+31871insAAGAGAGAGAGATCTAATTTTTACATTGTCCTCTAAAAGAATCCTAATCTGATCCAAGCAAGTCTGTCATGACCAAA	NP_001161792.1:n.-18+31870_-18+31871insAAGAGAGAGAGATCTAATTTTT...