Canonical Allele Identifier: CA2439980866

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80027115G= , CM000685.2:g.80027115G=	GRCh38
NC_000023.10:g.79282614G= , CM000685.1:g.79282614G=	GRCh37
NC_000023.9:g.79169270G=	NCBI36
NG_008998.1:g.17360G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.799-141G= MANE Select	ENSP00000362393.3:n.799-141G=
ENST00000373294.8:c.799-141G=	ENSP00000362390.5:n.799-141G=
ENST00000373296.7:c.799-141G=	ENSP00000362393.3:n.799-141G=
ENST00000626498.2:c.*411-141G=	ENSP00000487527.1:n.*411-141G=
ENST00000626877.1:n.678-141G=
NM_001109878.1:c.799-141G=	NP_001103348.1:n.799-141G=
NM_001109879.1:c.439-141G=	NP_001103349.1:n.439-141G=
NM_001303475.1:c.439-141G=	NP_001290404.1:n.439-141G=
NM_016954.2:c.799-141G=	NP_058650.1:n.799-141G=
XM_005262136.2:c.802-141G=	XP_005262193.1:n.802-141G=
XM_006724657.2:c.802-141G=	XP_006724720.1:n.802-141G=
XM_011530972.1:c.439-141G=	XP_011529274.1:n.439-141G=
NM_001109878.2:c.799-141G= MANE Select	NP_001103348.1:n.799-141G=
NM_001109879.2:c.439-141G=	NP_001103349.1:n.439-141G=