Canonical Allele Identifier: CA2439980819

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026984_80026985delinsGT , CM000685.2:g.80026984_80026985delinsGT	GRCh38
NC_000023.10:g.79282483_79282484delinsGT , CM000685.1:g.79282483_79282484delinsGT	GRCh37
NC_000023.9:g.79169139_79169140delinsGT	NCBI36
NG_008998.1:g.17229_17230delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.798+116_798+117delinsGT MANE Select	ENSP00000362393.3:n.798+116_798+117delinsGT
ENST00000373294.8:c.798+116_798+117delinsGT	ENSP00000362390.5:n.798+116_798+117delinsGT
ENST00000373296.7:c.798+116_798+117delinsGT	ENSP00000362393.3:n.798+116_798+117delinsGT
ENST00000626498.2:c.*410+116_*410+117delinsGT	ENSP00000487527.1:n.*410+116_*410+117delinsGT
ENST00000626877.1:n.677+116_677+117delinsGT
NM_001109878.1:c.798+116_798+117delinsGT	NP_001103348.1:n.798+116_798+117delinsGT
NM_001109879.1:c.438+116_438+117delinsGT	NP_001103349.1:n.438+116_438+117delinsGT
NM_001303475.1:c.438+116_438+117delinsGT	NP_001290404.1:n.438+116_438+117delinsGT
NM_016954.2:c.798+116_798+117delinsGT	NP_058650.1:n.798+116_798+117delinsGT
XM_005262136.2:c.801+116_801+117delinsGT	XP_005262193.1:n.801+116_801+117delinsGT
XM_006724657.2:c.801+116_801+117delinsGT	XP_006724720.1:n.801+116_801+117delinsGT
XM_011530972.1:c.438+116_438+117delinsGT	XP_011529274.1:n.438+116_438+117delinsGT
NM_001109878.2:c.798+116_798+117delinsGT MANE Select	NP_001103348.1:n.798+116_798+117delinsGT
NM_001109879.2:c.438+116_438+117delinsGT	NP_001103349.1:n.438+116_438+117delinsGT