Canonical Allele Identifier: CA2439980767

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026799T= , CM000685.2:g.80026799T=	GRCh38
NC_000023.10:g.79282298T= , CM000685.1:g.79282298T=	GRCh37
NC_000023.9:g.79168954T=	NCBI36
NG_008998.1:g.17044T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.729T= MANE Select	ENSP00000362393.3:p.Thr243=
ENST00000373294.8:c.729T=	ENSP00000362390.5:p.Thr243=
ENST00000373296.7:c.729T=	ENSP00000362393.3:p.Thr243=
ENST00000626498.2:c.*341T=	ENSP00000487527.1:n.*341T=
ENST00000626877.1:n.608T=
NM_001109878.1:c.729T=	NP_001103348.1:p.Thr243=
NM_001109879.1:c.369T=	NP_001103349.1:p.Thr123=
NM_001303475.1:c.369T=	NP_001290404.1:p.Thr123=
NM_016954.2:c.729T=	NP_058650.1:p.Thr243=
XM_005262136.2:c.732T=	XP_005262193.1:p.Thr244=
XM_006724657.2:c.732T=	XP_006724720.1:p.Thr244=
XM_011530972.1:c.369T=	XP_011529274.1:p.Thr123=
NM_001109878.2:c.729T= MANE Select	NP_001103348.1:p.Thr243=
NM_001109879.2:c.369T=	NP_001103349.1:p.Thr123=