Canonical Allele Identifier: CA944145873

Gene: TSPAN9

Linked Data

• gnomAD v3: 12-3108955-T-TTTTTCA
• gnomAD v4: 12-3108955-T-TTTTTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108955_3108956insTTTTCA , CM000674.2:g.3108955_3108956insTTTTCA	GRCh38
NC_000012.11:g.3218121_3218122insTTTTCA , CM000674.1:g.3218121_3218122insTTTTCA	GRCh37
NC_000012.10:g.3088382_3088383insTTTTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25236_-18+25237insTTTTCA MANE Select	ENSP00000011898.5:n.-18+25236_-18+25237insTTTTCA
ENST00000649909.1:c.-130+25236_-130+25237insTTTTCA	ENSP00000497370.1:n.-130+25236_-130+25237insTTTTCA
ENST00000011898.9:c.-18+25236_-18+25237insTTTTCA	ENSP00000011898.5:n.-18+25236_-18+25237insTTTTCA
ENST00000444315.6:c.-18+25236_-18+25237insTTTTCA	ENSP00000412908.2:n.-18+25236_-18+25237insTTTTCA
ENST00000537971.5:c.-18+31502_-18+31503insTTTTCA	ENSP00000444799.1:n.-18+31502_-18+31503insTTTTCA
NM_001168320.1:c.-18+31502_-18+31503insTTTTCA	NP_001161792.1:n.-18+31502_-18+31503insTTTTCA
NM_006675.4:c.-18+25236_-18+25237insTTTTCA	NP_006666.1:n.-18+25236_-18+25237insTTTTCA
XM_011520912.1:c.-349+25236_-349+25237insTTTTCA	XP_011519214.1:n.-349+25236_-349+25237insTTTTCA
XM_011520912.3:c.-349+25236_-349+25237insTTTTCA	XP_011519214.1:n.-349+25236_-349+25237insTTTTCA
NM_006675.5:c.-18+25236_-18+25237insTTTTCA MANE Select	NP_006666.1:n.-18+25236_-18+25237insTTTTCA
NM_001168320.2:c.-18+31502_-18+31503insTTTTCA	NP_001161792.1:n.-18+31502_-18+31503insTTTTCA