Canonical Allele Identifier: CA232005698

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1010652794
• gnomAD v2: 12-3218126-CAG-C
• gnomAD v3: 12-3108960-CAG-C
• gnomAD v4: 12-3108960-CAG-C
• MyVariant Identifiers: chr12:g.3218127_3218128del (hg19) ; chr12:g.3108961_3108962del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108963_3108964del , CM000674.2:g.3108963_3108964del	GRCh38
NC_000012.11:g.3218129_3218130del , CM000674.1:g.3218129_3218130del	GRCh37
NC_000012.10:g.3088390_3088391del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25244_-18+25245del MANE Select	ENSP00000011898.5:n.-18+25244_-18+25245del
ENST00000649909.1:c.-130+25244_-130+25245del	ENSP00000497370.1:n.-130+25244_-130+25245del
ENST00000011898.9:c.-18+25244_-18+25245del	ENSP00000011898.5:n.-18+25244_-18+25245del
ENST00000444315.6:c.-18+25244_-18+25245del	ENSP00000412908.2:n.-18+25244_-18+25245del
ENST00000537971.5:c.-18+31510_-18+31511del	ENSP00000444799.1:n.-18+31510_-18+31511del
NM_001168320.1:c.-18+31510_-18+31511del	NP_001161792.1:n.-18+31510_-18+31511del
NM_006675.4:c.-18+25244_-18+25245del	NP_006666.1:n.-18+25244_-18+25245del
XM_011520912.1:c.-349+25244_-349+25245del	XP_011519214.1:n.-349+25244_-349+25245del
XM_011520912.3:c.-349+25244_-349+25245del	XP_011519214.1:n.-349+25244_-349+25245del
NM_006675.5:c.-18+25244_-18+25245del MANE Select	NP_006666.1:n.-18+25244_-18+25245del
NM_001168320.2:c.-18+31510_-18+31511del	NP_001161792.1:n.-18+31510_-18+31511del