Canonical Allele Identifier: CA10461277

Gene: TBX22

Linked Data

• dbSNP Id: rs746197578
• ExAC: X:79282195 TC / T
• gnomAD v2: X-79282195-TC-T
• MyVariant Identifiers: chrX:g.79282196del (hg19) ; chrX:g.80026698del (hg38) ; chrX:g.80026697del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026698del , CM000685.2:g.80026698del	GRCh38
NC_000023.10:g.79282197del , CM000685.1:g.79282197del	GRCh37
NC_000023.9:g.79168853del	NCBI36
NG_008998.1:g.16943del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.634-6del MANE Select	ENSP00000362393.3:n.634-6del
ENST00000373294.8:c.634-6del	ENSP00000362390.5:n.634-6del
ENST00000373296.7:c.634-6del	ENSP00000362393.3:n.634-6del
ENST00000626498.2:c.*246-6del	ENSP00000487527.1:n.*246-6del
ENST00000626877.1:n.513-6del
NM_001109878.1:c.634-6del	NP_001103348.1:n.634-6del
NM_001109879.1:c.274-6del	NP_001103349.1:n.274-6del
NM_001303475.1:c.274-6del	NP_001290404.1:n.274-6del
NM_016954.2:c.634-6del	NP_058650.1:n.634-6del
XM_005262136.2:c.637-6del	XP_005262193.1:n.637-6del
XM_006724657.2:c.637-6del	XP_006724720.1:n.637-6del
XM_011530972.1:c.274-6del	XP_011529274.1:n.274-6del
NM_001109878.2:c.634-6del MANE Select	NP_001103348.1:n.634-6del
NM_001109879.2:c.274-6del	NP_001103349.1:n.274-6del