Canonical Allele Identifier: CA2439980770

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026817_80026818delinsCT , CM000685.2:g.80026817_80026818delinsCT	GRCh38
NC_000023.10:g.79282316_79282317delinsCT , CM000685.1:g.79282316_79282317delinsCT	GRCh37
NC_000023.9:g.79168972_79168973delinsCT	NCBI36
NG_008998.1:g.17062_17063delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.747_748delinsCT MANE Select	ENSP00000362393.3:p.Phe249=
ENST00000373294.8:c.747_748delinsCT	ENSP00000362390.5:p.Phe249=
ENST00000373296.7:c.747_748delinsCT	ENSP00000362393.3:p.Phe249=
ENST00000626498.2:c.*359_*360delinsCT	ENSP00000487527.1:n.*359_*360delinsCT
ENST00000626877.1:n.626_627delinsCT
NM_001109878.1:c.747_748delinsCT	NP_001103348.1:p.Phe249=
NM_001109879.1:c.387_388delinsCT	NP_001103349.1:p.Phe129=
NM_001303475.1:c.387_388delinsCT	NP_001290404.1:p.Phe129=
NM_016954.2:c.747_748delinsCT	NP_058650.1:p.Phe249=
XM_005262136.2:c.750_751delinsCT	XP_005262193.1:p.Phe250=
XM_006724657.2:c.750_751delinsCT	XP_006724720.1:p.Phe250=
XM_011530972.1:c.387_388delinsCT	XP_011529274.1:p.Phe129=
NM_001109878.2:c.747_748delinsCT MANE Select	NP_001103348.1:p.Phe249=
NM_001109879.2:c.387_388delinsCT	NP_001103349.1:p.Phe129=