Canonical Allele Identifier: CA944145895

Gene: TSPAN9

Linked Data

• dbSNP Id: rs2098316166
• gnomAD v3: 12-3108974-T-TC
• gnomAD v4: 12-3108974-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108974_3108975insC , CM000674.2:g.3108974_3108975insC	GRCh38
NC_000012.11:g.3218140_3218141insC , CM000674.1:g.3218140_3218141insC	GRCh37
NC_000012.10:g.3088401_3088402insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25255_-18+25256insC MANE Select	ENSP00000011898.5:n.-18+25255_-18+25256insC
ENST00000649909.1:c.-130+25255_-130+25256insC	ENSP00000497370.1:n.-130+25255_-130+25256insC
ENST00000011898.9:c.-18+25255_-18+25256insC	ENSP00000011898.5:n.-18+25255_-18+25256insC
ENST00000444315.6:c.-18+25255_-18+25256insC	ENSP00000412908.2:n.-18+25255_-18+25256insC
ENST00000537971.5:c.-18+31521_-18+31522insC	ENSP00000444799.1:n.-18+31521_-18+31522insC
NM_001168320.1:c.-18+31521_-18+31522insC	NP_001161792.1:n.-18+31521_-18+31522insC
NM_006675.4:c.-18+25255_-18+25256insC	NP_006666.1:n.-18+25255_-18+25256insC
XM_011520912.1:c.-349+25255_-349+25256insC	XP_011519214.1:n.-349+25255_-349+25256insC
XM_011520912.3:c.-349+25255_-349+25256insC	XP_011519214.1:n.-349+25255_-349+25256insC
NM_006675.5:c.-18+25255_-18+25256insC MANE Select	NP_006666.1:n.-18+25255_-18+25256insC
NM_001168320.2:c.-18+31521_-18+31522insC	NP_001161792.1:n.-18+31521_-18+31522insC