Canonical Allele Identifier: CA13611328

Gene: TSPAN9

Linked Data

• dbSNP Id: rs150269838
• gnomAD v2: 12-3218353-T-C
• gnomAD v3: 12-3109187-T-C
• gnomAD v4: 12-3109187-T-C
• MyVariant Identifiers: chr12:g.3218353T>C (hg19) ; chr12:g.3109187T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109187T>C , CM000674.2:g.3109187T>C	GRCh38
NC_000012.11:g.3218353T>C , CM000674.1:g.3218353T>C	GRCh37
NC_000012.10:g.3088614T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25468T>C MANE Select	ENSP00000011898.5:n.-18+25468T>C
ENST00000649909.1:c.-130+25468T>C	ENSP00000497370.1:n.-130+25468T>C
ENST00000011898.9:c.-18+25468T>C	ENSP00000011898.5:n.-18+25468T>C
ENST00000444315.6:c.-18+25468T>C	ENSP00000412908.2:n.-18+25468T>C
ENST00000537971.5:c.-18+31734T>C	ENSP00000444799.1:n.-18+31734T>C
NM_001168320.1:c.-18+31734T>C	NP_001161792.1:n.-18+31734T>C
NM_006675.4:c.-18+25468T>C	NP_006666.1:n.-18+25468T>C
XM_011520912.1:c.-349+25468T>C	XP_011519214.1:n.-349+25468T>C
XM_011520912.3:c.-349+25468T>C	XP_011519214.1:n.-349+25468T>C
NM_006675.5:c.-18+25468T>C MANE Select	NP_006666.1:n.-18+25468T>C
NM_001168320.2:c.-18+31734T>C	NP_001161792.1:n.-18+31734T>C