Canonical Allele Identifier: CA944145865

Gene: TSPAN9

Linked Data

• gnomAD v3: 12-3108943-CTTT-C
• gnomAD v4: 12-3108943-CTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108953_3108955del , CM000674.2:g.3108953_3108955del	GRCh38
NC_000012.11:g.3218119_3218121del , CM000674.1:g.3218119_3218121del	GRCh37
NC_000012.10:g.3088380_3088382del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25234_-18+25236del MANE Select	ENSP00000011898.5:n.-18+25234_-18+25236del
ENST00000649909.1:c.-130+25234_-130+25236del	ENSP00000497370.1:n.-130+25234_-130+25236del
ENST00000011898.9:c.-18+25234_-18+25236del	ENSP00000011898.5:n.-18+25234_-18+25236del
ENST00000444315.6:c.-18+25234_-18+25236del	ENSP00000412908.2:n.-18+25234_-18+25236del
ENST00000537971.5:c.-18+31500_-18+31502del	ENSP00000444799.1:n.-18+31500_-18+31502del
NM_001168320.1:c.-18+31500_-18+31502del	NP_001161792.1:n.-18+31500_-18+31502del
NM_006675.4:c.-18+25234_-18+25236del	NP_006666.1:n.-18+25234_-18+25236del
XM_011520912.1:c.-349+25234_-349+25236del	XP_011519214.1:n.-349+25234_-349+25236del
XM_011520912.3:c.-349+25234_-349+25236del	XP_011519214.1:n.-349+25234_-349+25236del
NM_006675.5:c.-18+25234_-18+25236del MANE Select	NP_006666.1:n.-18+25234_-18+25236del
NM_001168320.2:c.-18+31500_-18+31502del	NP_001161792.1:n.-18+31500_-18+31502del