Canonical Allele Identifier: CA687272214

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1241344213
• MyVariant Identifiers: chr12:g.3218291_3218292insA (hg19) ; chr12:g.3109125_3109126insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109125_3109126insA , CM000674.2:g.3109125_3109126insA	GRCh38
NC_000012.11:g.3218291_3218292insA , CM000674.1:g.3218291_3218292insA	GRCh37
NC_000012.10:g.3088552_3088553insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25406_-18+25407insA MANE Select	ENSP00000011898.5:n.-18+25406_-18+25407insA
ENST00000649909.1:c.-130+25406_-130+25407insA	ENSP00000497370.1:n.-130+25406_-130+25407insA
ENST00000011898.9:c.-18+25406_-18+25407insA	ENSP00000011898.5:n.-18+25406_-18+25407insA
ENST00000444315.6:c.-18+25406_-18+25407insA	ENSP00000412908.2:n.-18+25406_-18+25407insA
ENST00000537971.5:c.-18+31672_-18+31673insA	ENSP00000444799.1:n.-18+31672_-18+31673insA
NM_001168320.1:c.-18+31672_-18+31673insA	NP_001161792.1:n.-18+31672_-18+31673insA
NM_006675.4:c.-18+25406_-18+25407insA	NP_006666.1:n.-18+25406_-18+25407insA
XM_011520912.1:c.-349+25406_-349+25407insA	XP_011519214.1:n.-349+25406_-349+25407insA
XM_011520912.3:c.-349+25406_-349+25407insA	XP_011519214.1:n.-349+25406_-349+25407insA
NM_006675.5:c.-18+25406_-18+25407insA MANE Select	NP_006666.1:n.-18+25406_-18+25407insA
NM_001168320.2:c.-18+31672_-18+31673insA	NP_001161792.1:n.-18+31672_-18+31673insA