Canonical Allele Identifier: CA687272424

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1431808505
• gnomAD v2: 12-3218361-C-G
• gnomAD v3: 12-3109195-C-G
• gnomAD v4: 12-3109195-C-G
• MyVariant Identifiers: chr12:g.3218361C>G (hg19) ; chr12:g.3109195C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109195C>G , CM000674.2:g.3109195C>G	GRCh38
NC_000012.11:g.3218361C>G , CM000674.1:g.3218361C>G	GRCh37
NC_000012.10:g.3088622C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25476C>G MANE Select	ENSP00000011898.5:n.-18+25476C>G
ENST00000649909.1:c.-130+25476C>G	ENSP00000497370.1:n.-130+25476C>G
ENST00000011898.9:c.-18+25476C>G	ENSP00000011898.5:n.-18+25476C>G
ENST00000444315.6:c.-18+25476C>G	ENSP00000412908.2:n.-18+25476C>G
ENST00000537971.5:c.-18+31742C>G	ENSP00000444799.1:n.-18+31742C>G
NM_001168320.1:c.-18+31742C>G	NP_001161792.1:n.-18+31742C>G
NM_006675.4:c.-18+25476C>G	NP_006666.1:n.-18+25476C>G
XM_011520912.1:c.-349+25476C>G	XP_011519214.1:n.-349+25476C>G
XM_011520912.3:c.-349+25476C>G	XP_011519214.1:n.-349+25476C>G
NM_006675.5:c.-18+25476C>G MANE Select	NP_006666.1:n.-18+25476C>G
NM_001168320.2:c.-18+31742C>G	NP_001161792.1:n.-18+31742C>G