Canonical Allele Identifier: CA331778212

Gene: TBX22

Linked Data

• dbSNP Id: rs1055128403
• gnomAD v3: X-80027127-CATTT-C
• gnomAD v4: X-80027127-CATTT-C
• MyVariant Identifiers: chrX:g.79282627_79282630del (hg19) ; chrX:g.80027128_80027131del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80027133_80027136del , CM000685.2:g.80027133_80027136del	GRCh38
NC_000023.10:g.79282632_79282635del , CM000685.1:g.79282632_79282635del	GRCh37
NC_000023.9:g.79169288_79169291del	NCBI36
NG_008998.1:g.17378_17381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.799-123_799-120del MANE Select	ENSP00000362393.3:n.799-123_799-120del
ENST00000373294.8:c.799-123_799-120del	ENSP00000362390.5:n.799-123_799-120del
ENST00000373296.7:c.799-123_799-120del	ENSP00000362393.3:n.799-123_799-120del
ENST00000626498.2:c.*411-123_*411-120del	ENSP00000487527.1:n.*411-123_*411-120del
ENST00000626877.1:n.678-123_678-120del
NM_001109878.1:c.799-123_799-120del	NP_001103348.1:n.799-123_799-120del
NM_001109879.1:c.439-123_439-120del	NP_001103349.1:n.439-123_439-120del
NM_001303475.1:c.439-123_439-120del	NP_001290404.1:n.439-123_439-120del
NM_016954.2:c.799-123_799-120del	NP_058650.1:n.799-123_799-120del
XM_005262136.2:c.802-123_802-120del	XP_005262193.1:n.802-123_802-120del
XM_006724657.2:c.802-123_802-120del	XP_006724720.1:n.802-123_802-120del
XM_011530972.1:c.439-123_439-120del	XP_011529274.1:n.439-123_439-120del
NM_001109878.2:c.799-123_799-120del MANE Select	NP_001103348.1:n.799-123_799-120del
NM_001109879.2:c.439-123_439-120del	NP_001103349.1:n.439-123_439-120del