Canonical Allele Identifier: CA687272651

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1191879731
• gnomAD v3: 12-3109279-TGTGTGTGTGTGTGTGTGTGTGAGAGAGA-T
• gnomAD v4: 12-3109279-TGTGTGTGTGTGTGTGTGTGTGAGAGAGA-T
• MyVariant Identifiers: chr12:g.3218446_3218473del (hg19) ; chr12:g.3109280_3109307del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109300_3109327del , CM000674.2:g.3109300_3109327del	GRCh38
NC_000012.11:g.3218466_3218493del , CM000674.1:g.3218466_3218493del	GRCh37
NC_000012.10:g.3088727_3088754del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25581_-18+25608del MANE Select	ENSP00000011898.5:n.-18+25581_-18+25608del
ENST00000649909.1:c.-130+25581_-130+25608del	ENSP00000497370.1:n.-130+25581_-130+25608del
ENST00000011898.9:c.-18+25581_-18+25608del	ENSP00000011898.5:n.-18+25581_-18+25608del
ENST00000444315.6:c.-18+25581_-18+25608del	ENSP00000412908.2:n.-18+25581_-18+25608del
ENST00000537971.5:c.-18+31847_-18+31874del	ENSP00000444799.1:n.-18+31847_-18+31874del
NM_001168320.1:c.-18+31847_-18+31874del	NP_001161792.1:n.-18+31847_-18+31874del
NM_006675.4:c.-18+25581_-18+25608del	NP_006666.1:n.-18+25581_-18+25608del
XM_011520912.1:c.-349+25581_-349+25608del	XP_011519214.1:n.-349+25581_-349+25608del
XM_011520912.3:c.-349+25581_-349+25608del	XP_011519214.1:n.-349+25581_-349+25608del
NM_006675.5:c.-18+25581_-18+25608del MANE Select	NP_006666.1:n.-18+25581_-18+25608del
NM_001168320.2:c.-18+31847_-18+31874del	NP_001161792.1:n.-18+31847_-18+31874del