Canonical Allele Identifier: CA2822025073

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026840_80026841insACCCAA , CM000685.2:g.80026840_80026841insACCCAA	GRCh38
NC_000023.10:g.79282339_79282340insACCCAA , CM000685.1:g.79282339_79282340insACCCAA	GRCh37
NC_000023.9:g.79168995_79168996insACCCAA	NCBI36
NG_008998.1:g.17085_17086insACCCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.770_771insACCCAA MANE Select	ENSP00000362393.3:p.Thr257_Thr258insProAsn
ENST00000373294.8:c.770_771insACCCAA	ENSP00000362390.5:p.Thr257_Thr258insProAsn
ENST00000373296.7:c.770_771insACCCAA	ENSP00000362393.3:p.Thr257_Thr258insProAsn
ENST00000626498.2:c.*382_*383insACCCAA	ENSP00000487527.1:n.*382_*383insACCCAA
ENST00000626877.1:n.649_650insACCCAA
NM_001109878.1:c.770_771insACCCAA	NP_001103348.1:p.Thr257_Thr258insProAsn
NM_001109879.1:c.410_411insACCCAA	NP_001103349.1:p.Thr137_Thr138insProAsn
NM_001303475.1:c.410_411insACCCAA	NP_001290404.1:p.Thr137_Thr138insProAsn
NM_016954.2:c.770_771insACCCAA	NP_058650.1:p.Thr257_Thr258insProAsn
XM_005262136.2:c.773_774insACCCAA	XP_005262193.1:p.Thr258_Thr259insProAsn
XM_006724657.2:c.773_774insACCCAA	XP_006724720.1:p.Thr258_Thr259insProAsn
XM_011530972.1:c.410_411insACCCAA	XP_011529274.1:p.Thr137_Thr138insProAsn
NM_001109878.2:c.770_771insACCCAA MANE Select	NP_001103348.1:p.Thr257_Thr258insProAsn
NM_001109879.2:c.410_411insACCCAA	NP_001103349.1:p.Thr137_Thr138insProAsn