Canonical Allele Identifier: CA687273429

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1455233131
• MyVariant Identifiers: chr12:g.3218661_3218680del (hg19) ; chr12:g.3109495_3109514del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109497_3109516del , CM000674.2:g.3109497_3109516del	GRCh38
NC_000012.11:g.3218663_3218682del , CM000674.1:g.3218663_3218682del	GRCh37
NC_000012.10:g.3088924_3088943del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25778_-18+25797del MANE Select	ENSP00000011898.5:n.-18+25778_-18+25797del
ENST00000649909.1:c.-130+25778_-130+25797del	ENSP00000497370.1:n.-130+25778_-130+25797del
ENST00000011898.9:c.-18+25778_-18+25797del	ENSP00000011898.5:n.-18+25778_-18+25797del
ENST00000444315.6:c.-18+25778_-18+25797del	ENSP00000412908.2:n.-18+25778_-18+25797del
ENST00000537971.5:c.-18+32044_-18+32063del	ENSP00000444799.1:n.-18+32044_-18+32063del
NM_001168320.1:c.-18+32044_-18+32063del	NP_001161792.1:n.-18+32044_-18+32063del
NM_006675.4:c.-18+25778_-18+25797del	NP_006666.1:n.-18+25778_-18+25797del
XM_011520912.1:c.-349+25778_-349+25797del	XP_011519214.1:n.-349+25778_-349+25797del
XM_011520912.3:c.-349+25778_-349+25797del	XP_011519214.1:n.-349+25778_-349+25797del
NM_006675.5:c.-18+25778_-18+25797del MANE Select	NP_006666.1:n.-18+25778_-18+25797del
NM_001168320.2:c.-18+32044_-18+32063del	NP_001161792.1:n.-18+32044_-18+32063del