Canonical Allele Identifier: CA878635822

Gene: TBX22

Linked Data

• dbSNP Id: rs1282186149
• gnomAD v3: X-80026984-GT-G
• gnomAD v4: X-80026984-GT-G
• MyVariant Identifiers: chrX:g.79282484del (hg19) ; chrX:g.80026985del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026988del , CM000685.2:g.80026988del	GRCh38
NC_000023.10:g.79282487del , CM000685.1:g.79282487del	GRCh37
NC_000023.9:g.79169143del	NCBI36
NG_008998.1:g.17233del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.798+120del MANE Select	ENSP00000362393.3:n.798+120del
ENST00000373294.8:c.798+120del	ENSP00000362390.5:n.798+120del
ENST00000373296.7:c.798+120del	ENSP00000362393.3:n.798+120del
ENST00000626498.2:c.*410+120del	ENSP00000487527.1:n.*410+120del
ENST00000626877.1:n.677+120del
NM_001109878.1:c.798+120del	NP_001103348.1:n.798+120del
NM_001109879.1:c.438+120del	NP_001103349.1:n.438+120del
NM_001303475.1:c.438+120del	NP_001290404.1:n.438+120del
NM_016954.2:c.798+120del	NP_058650.1:n.798+120del
XM_005262136.2:c.801+120del	XP_005262193.1:n.801+120del
XM_006724657.2:c.801+120del	XP_006724720.1:n.801+120del
XM_011530972.1:c.438+120del	XP_011529274.1:n.438+120del
NM_001109878.2:c.798+120del MANE Select	NP_001103348.1:n.798+120del
NM_001109879.2:c.438+120del	NP_001103349.1:n.438+120del