Canonical Allele Identifier: CA413740660

Gene: TBX22

Linked Data

• MyVariant Identifiers: chrX:g.79282225A>C (hg19) ; chrX:g.80026726A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026726A>C , CM000685.2:g.80026726A>C	GRCh38
NC_000023.10:g.79282225A>C , CM000685.1:g.79282225A>C	GRCh37
NC_000023.9:g.79168881A>C	NCBI36
NG_008998.1:g.16971A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.656A>C MANE Select	ENSP00000362393.3:p.Lys219Thr
ENST00000373294.8:c.656A>C	ENSP00000362390.5:p.Lys219Thr
ENST00000373296.7:c.656A>C	ENSP00000362393.3:p.Lys219Thr
ENST00000626498.2:c.*268A>C	ENSP00000487527.1:n.*268A>C
ENST00000626877.1:n.535A>C
NM_001109878.1:c.656A>C	NP_001103348.1:p.Lys219Thr
NM_001109879.1:c.296A>C	NP_001103349.1:p.Lys99Thr
NM_001303475.1:c.296A>C	NP_001290404.1:p.Lys99Thr
NM_016954.2:c.656A>C	NP_058650.1:p.Lys219Thr
XM_005262136.2:c.659A>C	XP_005262193.1:p.Lys220Thr
XM_006724657.2:c.659A>C	XP_006724720.1:p.Lys220Thr
XM_011530972.1:c.296A>C	XP_011529274.1:p.Lys99Thr
NM_001109878.2:c.656A>C MANE Select	NP_001103348.1:p.Lys219Thr
NM_001109879.2:c.296A>C	NP_001103349.1:p.Lys99Thr