Canonical Allele Identifier: CA944145866

Gene: TSPAN9

Linked Data

• dbSNP Id: rs879519277
• gnomAD v3: 12-3108943-C-CTT
• gnomAD v4: 12-3108943-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108954_3108955dup , CM000674.2:g.3108954_3108955dup	GRCh38
NC_000012.11:g.3218120_3218121dup , CM000674.1:g.3218120_3218121dup	GRCh37
NC_000012.10:g.3088381_3088382dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25235_-18+25236dup MANE Select	ENSP00000011898.5:n.-18+25235_-18+25236dup
ENST00000649909.1:c.-130+25235_-130+25236dup	ENSP00000497370.1:n.-130+25235_-130+25236dup
ENST00000011898.9:c.-18+25235_-18+25236dup	ENSP00000011898.5:n.-18+25235_-18+25236dup
ENST00000444315.6:c.-18+25235_-18+25236dup	ENSP00000412908.2:n.-18+25235_-18+25236dup
ENST00000537971.5:c.-18+31501_-18+31502dup	ENSP00000444799.1:n.-18+31501_-18+31502dup
NM_001168320.1:c.-18+31501_-18+31502dup	NP_001161792.1:n.-18+31501_-18+31502dup
NM_006675.4:c.-18+25235_-18+25236dup	NP_006666.1:n.-18+25235_-18+25236dup
XM_011520912.1:c.-349+25235_-349+25236dup	XP_011519214.1:n.-349+25235_-349+25236dup
XM_011520912.3:c.-349+25235_-349+25236dup	XP_011519214.1:n.-349+25235_-349+25236dup
NM_006675.5:c.-18+25235_-18+25236dup MANE Select	NP_006666.1:n.-18+25235_-18+25236dup
NM_001168320.2:c.-18+31501_-18+31502dup	NP_001161792.1:n.-18+31501_-18+31502dup