Canonical Allele Identifier: CA2012590618

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3178113G= , CM000674.2:g.3178113G=	GRCh38
NC_000012.11:g.3287279G= , CM000674.1:g.3287279G=	GRCh37
NC_000012.10:g.3157540G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-17-23064G= MANE Select	ENSP00000011898.5:n.-17-23064G=
ENST00000649909.1:c.-130+94394G=	ENSP00000497370.1:n.-130+94394G=
ENST00000011898.9:c.-17-23064G=	ENSP00000011898.5:n.-17-23064G=
ENST00000444315.6:c.-17-23064G=	ENSP00000412908.2:n.-17-23064G=
ENST00000537971.5:c.-17-23064G=	ENSP00000444799.1:n.-17-23064G=
NM_001168320.1:c.-17-23064G=	NP_001161792.1:n.-17-23064G=
NM_006675.4:c.-17-23064G=	NP_006666.1:n.-17-23064G=
XM_011520912.1:c.-348-23064G=	XP_011519214.1:n.-348-23064G=
XM_011520912.3:c.-348-23064G=	XP_011519214.1:n.-348-23064G=
NM_006675.5:c.-17-23064G= MANE Select	NP_006666.1:n.-17-23064G=
NM_001168320.2:c.-17-23064G=	NP_001161792.1:n.-17-23064G=