Canonical Allele Identifier: CA2439980870

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80027127_80027131delinsCATTT , CM000685.2:g.80027127_80027131delinsCATTT	GRCh38
NC_000023.10:g.79282626_79282630delinsCATTT , CM000685.1:g.79282626_79282630delinsCATTT	GRCh37
NC_000023.9:g.79169282_79169286delinsCATTT	NCBI36
NG_008998.1:g.17372_17376delinsCATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.799-129_799-125delinsCATTT MANE Select	ENSP00000362393.3:n.799-129_799-125delinsCATTT
ENST00000373294.8:c.799-129_799-125delinsCATTT	ENSP00000362390.5:n.799-129_799-125delinsCATTT
ENST00000373296.7:c.799-129_799-125delinsCATTT	ENSP00000362393.3:n.799-129_799-125delinsCATTT
ENST00000626498.2:c.*411-129_*411-125delinsCATTT	ENSP00000487527.1:n.*411-129_*411-125delinsCATTT
ENST00000626877.1:n.678-129_678-125delinsCATTT
NM_001109878.1:c.799-129_799-125delinsCATTT	NP_001103348.1:n.799-129_799-125delinsCATTT
NM_001109879.1:c.439-129_439-125delinsCATTT	NP_001103349.1:n.439-129_439-125delinsCATTT
NM_001303475.1:c.439-129_439-125delinsCATTT	NP_001290404.1:n.439-129_439-125delinsCATTT
NM_016954.2:c.799-129_799-125delinsCATTT	NP_058650.1:n.799-129_799-125delinsCATTT
XM_005262136.2:c.802-129_802-125delinsCATTT	XP_005262193.1:n.802-129_802-125delinsCATTT
XM_006724657.2:c.802-129_802-125delinsCATTT	XP_006724720.1:n.802-129_802-125delinsCATTT
XM_011530972.1:c.439-129_439-125delinsCATTT	XP_011529274.1:n.439-129_439-125delinsCATTT
NM_001109878.2:c.799-129_799-125delinsCATTT MANE Select	NP_001103348.1:n.799-129_799-125delinsCATTT
NM_001109879.2:c.439-129_439-125delinsCATTT	NP_001103349.1:n.439-129_439-125delinsCATTT