Canonical Allele Identifier: CA2439980738

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026715A= , CM000685.2:g.80026715A=	GRCh38
NC_000023.10:g.79282214A= , CM000685.1:g.79282214A=	GRCh37
NC_000023.9:g.79168870A=	NCBI36
NG_008998.1:g.16960A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.645A= MANE Select	ENSP00000362393.3:p.Gln215=
ENST00000373294.8:c.645A=	ENSP00000362390.5:p.Gln215=
ENST00000373296.7:c.645A=	ENSP00000362393.3:p.Gln215=
ENST00000626498.2:c.*257A=	ENSP00000487527.1:n.*257A=
ENST00000626877.1:n.524A=
NM_001109878.1:c.645A=	NP_001103348.1:p.Gln215=
NM_001109879.1:c.285A=	NP_001103349.1:p.Gln95=
NM_001303475.1:c.285A=	NP_001290404.1:p.Gln95=
NM_016954.2:c.645A=	NP_058650.1:p.Gln215=
XM_005262136.2:c.648A=	XP_005262193.1:p.Gln216=
XM_006724657.2:c.648A=	XP_006724720.1:p.Gln216=
XM_011530972.1:c.285A=	XP_011529274.1:p.Gln95=
NM_001109878.2:c.645A= MANE Select	NP_001103348.1:p.Gln215=
NM_001109879.2:c.285A=	NP_001103349.1:p.Gln95=