Canonical Allele Identifier: CA2012557247

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109049_3109050delinsTC , CM000674.2:g.3109049_3109050delinsTC	GRCh38
NC_000012.11:g.3218215_3218216delinsTC , CM000674.1:g.3218215_3218216delinsTC	GRCh37
NC_000012.10:g.3088476_3088477delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25330_-18+25331delinsTC MANE Select	ENSP00000011898.5:n.-18+25330_-18+25331delinsTC
ENST00000649909.1:c.-130+25330_-130+25331delinsTC	ENSP00000497370.1:n.-130+25330_-130+25331delinsTC
ENST00000011898.9:c.-18+25330_-18+25331delinsTC	ENSP00000011898.5:n.-18+25330_-18+25331delinsTC
ENST00000444315.6:c.-18+25330_-18+25331delinsTC	ENSP00000412908.2:n.-18+25330_-18+25331delinsTC
ENST00000537971.5:c.-18+31596_-18+31597delinsTC	ENSP00000444799.1:n.-18+31596_-18+31597delinsTC
NM_001168320.1:c.-18+31596_-18+31597delinsTC	NP_001161792.1:n.-18+31596_-18+31597delinsTC
NM_006675.4:c.-18+25330_-18+25331delinsTC	NP_006666.1:n.-18+25330_-18+25331delinsTC
XM_011520912.1:c.-349+25330_-349+25331delinsTC	XP_011519214.1:n.-349+25330_-349+25331delinsTC
XM_011520912.3:c.-349+25330_-349+25331delinsTC	XP_011519214.1:n.-349+25330_-349+25331delinsTC
NM_006675.5:c.-18+25330_-18+25331delinsTC MANE Select	NP_006666.1:n.-18+25330_-18+25331delinsTC
NM_001168320.2:c.-18+31596_-18+31597delinsTC	NP_001161792.1:n.-18+31596_-18+31597delinsTC