Canonical Allele Identifier: CA687271910

Gene: TSPAN9

Linked Data

• dbSNP Id: rs1316003027
• gnomAD v3: 12-3108972-C-CAG
• gnomAD v4: 12-3108972-C-CAG
• MyVariant Identifiers: chr12:g.3218138_3218139insAG (hg19) ; chr12:g.3108972_3108973insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108972_3108973insAG , CM000674.2:g.3108972_3108973insAG	GRCh38
NC_000012.11:g.3218138_3218139insAG , CM000674.1:g.3218138_3218139insAG	GRCh37
NC_000012.10:g.3088399_3088400insAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25253_-18+25254insAG MANE Select	ENSP00000011898.5:n.-18+25253_-18+25254insAG
ENST00000649909.1:c.-130+25253_-130+25254insAG	ENSP00000497370.1:n.-130+25253_-130+25254insAG
ENST00000011898.9:c.-18+25253_-18+25254insAG	ENSP00000011898.5:n.-18+25253_-18+25254insAG
ENST00000444315.6:c.-18+25253_-18+25254insAG	ENSP00000412908.2:n.-18+25253_-18+25254insAG
ENST00000537971.5:c.-18+31519_-18+31520insAG	ENSP00000444799.1:n.-18+31519_-18+31520insAG
NM_001168320.1:c.-18+31519_-18+31520insAG	NP_001161792.1:n.-18+31519_-18+31520insAG
NM_006675.4:c.-18+25253_-18+25254insAG	NP_006666.1:n.-18+25253_-18+25254insAG
XM_011520912.1:c.-349+25253_-349+25254insAG	XP_011519214.1:n.-349+25253_-349+25254insAG
XM_011520912.3:c.-349+25253_-349+25254insAG	XP_011519214.1:n.-349+25253_-349+25254insAG
NM_006675.5:c.-18+25253_-18+25254insAG MANE Select	NP_006666.1:n.-18+25253_-18+25254insAG
NM_001168320.2:c.-18+31519_-18+31520insAG	NP_001161792.1:n.-18+31519_-18+31520insAG