Canonical Allele Identifier: CA413740931

Gene: TBX22

Linked Data

• MyVariant Identifiers: chrX:g.79282348C>G (hg19) ; chrX:g.80026849C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026849C>G , CM000685.2:g.80026849C>G	GRCh38
NC_000023.10:g.79282348C>G , CM000685.1:g.79282348C>G	GRCh37
NC_000023.9:g.79169004C>G	NCBI36
NG_008998.1:g.17094C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373296.8:c.779C>G MANE Select	ENSP00000362393.3:p.Thr260Arg
ENST00000373294.8:c.779C>G	ENSP00000362390.5:p.Thr260Arg
ENST00000373296.7:c.779C>G	ENSP00000362393.3:p.Thr260Arg
ENST00000626498.2:c.*391C>G	ENSP00000487527.1:n.*391C>G
ENST00000626877.1:n.658C>G
NM_001109878.1:c.779C>G	NP_001103348.1:p.Thr260Arg
NM_001109879.1:c.419C>G	NP_001103349.1:p.Thr140Arg
NM_001303475.1:c.419C>G	NP_001290404.1:p.Thr140Arg
NM_016954.2:c.779C>G	NP_058650.1:p.Thr260Arg
XM_005262136.2:c.782C>G	XP_005262193.1:p.Thr261Arg
XM_006724657.2:c.782C>G	XP_006724720.1:p.Thr261Arg
XM_011530972.1:c.419C>G	XP_011529274.1:p.Thr140Arg
NM_001109878.2:c.779C>G MANE Select	NP_001103348.1:p.Thr260Arg
NM_001109879.2:c.419C>G	NP_001103349.1:p.Thr140Arg