Canonical Allele Identifier: CA2521066915

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80025599_80025600del , CM000685.2:g.80025599_80025600del	GRCh38
NC_000023.10:g.79281098_79281099del , CM000685.1:g.79281098_79281099del	GRCh37
NC_000023.9:g.79167754_79167755del	NCBI36
NG_008998.1:g.15844_15845del

Transcript Alleles

HGVS	Amino-acid change
ENST00000373296.8:c.459-4_459-3del MANE Select	ENSP00000362393.3:n.459-4_459-3del
ENST00000373294.8:c.459-4_459-3del	ENSP00000362390.5:n.459-4_459-3del
ENST00000373296.7:c.459-4_459-3del	ENSP00000362393.3:n.459-4_459-3del
ENST00000626498.2:c.*71-4_*71-3del	ENSP00000487527.1:n.*71-4_*71-3del
ENST00000626877.1:n.338-4_338-3del
NM_001109878.1:c.459-4_459-3del	NP_001103348.1:n.459-4_459-3del
NM_001109879.1:c.99-4_99-3del	NP_001103349.1:n.99-4_99-3del
NM_001303475.1:c.99-4_99-3del	NP_001290404.1:n.99-4_99-3del
NM_016954.2:c.459-4_459-3del	NP_058650.1:n.459-4_459-3del
XM_005262136.2:c.462-4_462-3del	XP_005262193.1:n.462-4_462-3del
XM_006724657.2:c.462-4_462-3del	XP_006724720.1:n.462-4_462-3del
XM_011530972.1:c.99-4_99-3del	XP_011529274.1:n.99-4_99-3del
NM_001109878.2:c.459-4_459-3del MANE Select	NP_001103348.1:n.459-4_459-3del
NM_001109879.2:c.99-4_99-3del	NP_001103349.1:n.99-4_99-3del