Canonical Allele Identifier: CA413740437

Gene: TBX22

Linked Data

• MyVariant Identifiers: chrX:g.79281209G>C (hg19) ; chrX:g.80025710G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80025710G>C , CM000685.2:g.80025710G>C	GRCh38
NC_000023.10:g.79281209G>C , CM000685.1:g.79281209G>C	GRCh37
NC_000023.9:g.79167865G>C	NCBI36
NG_008998.1:g.15955G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.566G>C MANE Select	ENSP00000362393.3:p.Trp189Ser
ENST00000373294.8:c.566G>C	ENSP00000362390.5:p.Trp189Ser
ENST00000373296.7:c.566G>C	ENSP00000362393.3:p.Trp189Ser
ENST00000626498.2:c.*178G>C	ENSP00000487527.1:n.*178G>C
ENST00000626877.1:n.445G>C
NM_001109878.1:c.566G>C	NP_001103348.1:p.Trp189Ser
NM_001109879.1:c.206G>C	NP_001103349.1:p.Trp69Ser
NM_001303475.1:c.206G>C	NP_001290404.1:p.Trp69Ser
NM_016954.2:c.566G>C	NP_058650.1:p.Trp189Ser
XM_005262136.2:c.569G>C	XP_005262193.1:p.Trp190Ser
XM_006724657.2:c.569G>C	XP_006724720.1:p.Trp190Ser
XM_011530972.1:c.206G>C	XP_011529274.1:p.Trp69Ser
NM_001109878.2:c.566G>C MANE Select	NP_001103348.1:p.Trp189Ser
NM_001109879.2:c.206G>C	NP_001103349.1:p.Trp69Ser