Canonical Allele Identifier: CA2535200990

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108947_3108948insC , CM000674.2:g.3108947_3108948insC	GRCh38
NC_000012.11:g.3218113_3218114insC , CM000674.1:g.3218113_3218114insC	GRCh37
NC_000012.10:g.3088374_3088375insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25228_-18+25229insC MANE Select	ENSP00000011898.5:n.-18+25228_-18+25229insC
ENST00000649909.1:c.-130+25228_-130+25229insC	ENSP00000497370.1:n.-130+25228_-130+25229insC
ENST00000011898.9:c.-18+25228_-18+25229insC	ENSP00000011898.5:n.-18+25228_-18+25229insC
ENST00000444315.6:c.-18+25228_-18+25229insC	ENSP00000412908.2:n.-18+25228_-18+25229insC
ENST00000537971.5:c.-18+31494_-18+31495insC	ENSP00000444799.1:n.-18+31494_-18+31495insC
NM_001168320.1:c.-18+31494_-18+31495insC	NP_001161792.1:n.-18+31494_-18+31495insC
NM_006675.4:c.-18+25228_-18+25229insC	NP_006666.1:n.-18+25228_-18+25229insC
XM_011520912.1:c.-349+25228_-349+25229insC	XP_011519214.1:n.-349+25228_-349+25229insC
XM_011520912.3:c.-349+25228_-349+25229insC	XP_011519214.1:n.-349+25228_-349+25229insC
NM_006675.5:c.-18+25228_-18+25229insC MANE Select	NP_006666.1:n.-18+25228_-18+25229insC
NM_001168320.2:c.-18+31494_-18+31495insC	NP_001161792.1:n.-18+31494_-18+31495insC