Canonical Allele Identifier: CA2725619462

Gene: TSPAN9

Linked Data

• dbSNP Id: rs2153965124

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109087_3109088insTGCT , CM000674.2:g.3109087_3109088insTGCT	GRCh38
NC_000012.11:g.3218253_3218254insTGCT , CM000674.1:g.3218253_3218254insTGCT	GRCh37
NC_000012.10:g.3088514_3088515insTGCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25368_-18+25369insTGCT MANE Select	ENSP00000011898.5:n.-18+25368_-18+25369insTGCT
ENST00000649909.1:c.-130+25368_-130+25369insTGCT	ENSP00000497370.1:n.-130+25368_-130+25369insTGCT
ENST00000011898.9:c.-18+25368_-18+25369insTGCT	ENSP00000011898.5:n.-18+25368_-18+25369insTGCT
ENST00000444315.6:c.-18+25368_-18+25369insTGCT	ENSP00000412908.2:n.-18+25368_-18+25369insTGCT
ENST00000537971.5:c.-18+31634_-18+31635insTGCT	ENSP00000444799.1:n.-18+31634_-18+31635insTGCT
NM_001168320.1:c.-18+31634_-18+31635insTGCT	NP_001161792.1:n.-18+31634_-18+31635insTGCT
NM_006675.4:c.-18+25368_-18+25369insTGCT	NP_006666.1:n.-18+25368_-18+25369insTGCT
XM_011520912.1:c.-349+25368_-349+25369insTGCT	XP_011519214.1:n.-349+25368_-349+25369insTGCT
XM_011520912.3:c.-349+25368_-349+25369insTGCT	XP_011519214.1:n.-349+25368_-349+25369insTGCT
NM_006675.5:c.-18+25368_-18+25369insTGCT MANE Select	NP_006666.1:n.-18+25368_-18+25369insTGCT
NM_001168320.2:c.-18+31634_-18+31635insTGCT	NP_001161792.1:n.-18+31634_-18+31635insTGCT