Canonical Allele Identifier: CA2694191610

Gene: TBX22

Linked Data

• gnomAD v4: X-80026608-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026613del , CM000685.2:g.80026613del	GRCh38
NC_000023.10:g.79282112del , CM000685.1:g.79282112del	GRCh37
NC_000023.9:g.79168768del	NCBI36
NG_008998.1:g.16858del

Transcript Alleles

HGVS	Amino-acid change
ENST00000373296.8:c.634-91del MANE Select	ENSP00000362393.3:n.634-91del
ENST00000373294.8:c.634-91del	ENSP00000362390.5:n.634-91del
ENST00000373296.7:c.634-91del	ENSP00000362393.3:n.634-91del
ENST00000626498.2:c.*246-91del	ENSP00000487527.1:n.*246-91del
ENST00000626877.1:n.513-91del
NM_001109878.1:c.634-91del	NP_001103348.1:n.634-91del
NM_001109879.1:c.274-91del	NP_001103349.1:n.274-91del
NM_001303475.1:c.274-91del	NP_001290404.1:n.274-91del
NM_016954.2:c.634-91del	NP_058650.1:n.634-91del
XM_005262136.2:c.637-91del	XP_005262193.1:n.637-91del
XM_006724657.2:c.637-91del	XP_006724720.1:n.637-91del
XM_011530972.1:c.274-91del	XP_011529274.1:n.274-91del
NM_001109878.2:c.634-91del MANE Select	NP_001103348.1:n.634-91del
NM_001109879.2:c.274-91del	NP_001103349.1:n.274-91del