Canonical Allele Identifier: CA517403061

Gene: TBX22

Linked Data

• COSMIC: COSM3406617
• MyVariant Identifiers: chrX:g.79282295C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026796C>A , CM000685.2:g.80026796C>A	GRCh38
NC_000023.10:g.79282295C>A , CM000685.1:g.79282295C>A	GRCh37
NC_000023.9:g.79168951C>A	NCBI36
NG_008998.1:g.17041C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.726C>A MANE Select	ENSP00000362393.3:p.Pro242=
ENST00000373294.8:c.726C>A	ENSP00000362390.5:p.Pro242=
ENST00000373296.7:c.726C>A	ENSP00000362393.3:p.Pro242=
ENST00000626498.2:c.*338C>A	ENSP00000487527.1:n.*338C>A
ENST00000626877.1:n.605C>A
NM_001109878.1:c.726C>A	NP_001103348.1:p.Pro242=
NM_001109879.1:c.366C>A	NP_001103349.1:p.Pro122=
NM_001303475.1:c.366C>A	NP_001290404.1:p.Pro122=
NM_016954.2:c.726C>A	NP_058650.1:p.Pro242=
XM_005262136.2:c.729C>A	XP_005262193.1:p.Pro243=
XM_006724657.2:c.729C>A	XP_006724720.1:p.Pro243=
XM_011530972.1:c.366C>A	XP_011529274.1:p.Pro122=
NM_001109878.2:c.726C>A MANE Select	NP_001103348.1:p.Pro242=
NM_001109879.2:c.366C>A	NP_001103349.1:p.Pro122=