Canonical Allele Identifier: CA2012557478

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109265_3109269delinsAGTCT , CM000674.2:g.3109265_3109269delinsAGTCT	GRCh38
NC_000012.11:g.3218431_3218435delinsAGTCT , CM000674.1:g.3218431_3218435delinsAGTCT	GRCh37
NC_000012.10:g.3088692_3088696delinsAGTCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25546_-18+25550delinsAGTCT MANE Select	ENSP00000011898.5:n.-18+25546_-18+25550delinsAGTCT
ENST00000649909.1:c.-130+25546_-130+25550delinsAGTCT	ENSP00000497370.1:n.-130+25546_-130+25550delinsAGTCT
ENST00000011898.9:c.-18+25546_-18+25550delinsAGTCT	ENSP00000011898.5:n.-18+25546_-18+25550delinsAGTCT
ENST00000444315.6:c.-18+25546_-18+25550delinsAGTCT	ENSP00000412908.2:n.-18+25546_-18+25550delinsAGTCT
ENST00000537971.5:c.-18+31812_-18+31816delinsAGTCT	ENSP00000444799.1:n.-18+31812_-18+31816delinsAGTCT
NM_001168320.1:c.-18+31812_-18+31816delinsAGTCT	NP_001161792.1:n.-18+31812_-18+31816delinsAGTCT
NM_006675.4:c.-18+25546_-18+25550delinsAGTCT	NP_006666.1:n.-18+25546_-18+25550delinsAGTCT
XM_011520912.1:c.-349+25546_-349+25550delinsAGTCT	XP_011519214.1:n.-349+25546_-349+25550delinsAGTCT
XM_011520912.3:c.-349+25546_-349+25550delinsAGTCT	XP_011519214.1:n.-349+25546_-349+25550delinsAGTCT
NM_006675.5:c.-18+25546_-18+25550delinsAGTCT MANE Select	NP_006666.1:n.-18+25546_-18+25550delinsAGTCT
NM_001168320.2:c.-18+31812_-18+31816delinsAGTCT	NP_001161792.1:n.-18+31812_-18+31816delinsAGTCT