Canonical Allele Identifier: CA2525127347

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109315_3109316insTTGT , CM000674.2:g.3109315_3109316insTTGT	GRCh38
NC_000012.11:g.3218481_3218482insTTGT , CM000674.1:g.3218481_3218482insTTGT	GRCh37
NC_000012.10:g.3088742_3088743insTTGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25596_-18+25597insTTGT MANE Select	ENSP00000011898.5:n.-18+25596_-18+25597insTTGT
ENST00000649909.1:c.-130+25596_-130+25597insTTGT	ENSP00000497370.1:n.-130+25596_-130+25597insTTGT
ENST00000011898.9:c.-18+25596_-18+25597insTTGT	ENSP00000011898.5:n.-18+25596_-18+25597insTTGT
ENST00000444315.6:c.-18+25596_-18+25597insTTGT	ENSP00000412908.2:n.-18+25596_-18+25597insTTGT
ENST00000537971.5:c.-18+31862_-18+31863insTTGT	ENSP00000444799.1:n.-18+31862_-18+31863insTTGT
NM_001168320.1:c.-18+31862_-18+31863insTTGT	NP_001161792.1:n.-18+31862_-18+31863insTTGT
NM_006675.4:c.-18+25596_-18+25597insTTGT	NP_006666.1:n.-18+25596_-18+25597insTTGT
XM_011520912.1:c.-349+25596_-349+25597insTTGT	XP_011519214.1:n.-349+25596_-349+25597insTTGT
XM_011520912.3:c.-349+25596_-349+25597insTTGT	XP_011519214.1:n.-349+25596_-349+25597insTTGT
NM_006675.5:c.-18+25596_-18+25597insTTGT MANE Select	NP_006666.1:n.-18+25596_-18+25597insTTGT
NM_001168320.2:c.-18+31862_-18+31863insTTGT	NP_001161792.1:n.-18+31862_-18+31863insTTGT