Canonical Allele Identifier: CA2439980735

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026696_80026697delinsTC , CM000685.2:g.80026696_80026697delinsTC	GRCh38
NC_000023.10:g.79282195_79282196delinsTC , CM000685.1:g.79282195_79282196delinsTC	GRCh37
NC_000023.9:g.79168851_79168852delinsTC	NCBI36
NG_008998.1:g.16941_16942delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.634-8_634-7delinsTC MANE Select	ENSP00000362393.3:n.634-8_634-7delinsTC
ENST00000373294.8:c.634-8_634-7delinsTC	ENSP00000362390.5:n.634-8_634-7delinsTC
ENST00000373296.7:c.634-8_634-7delinsTC	ENSP00000362393.3:n.634-8_634-7delinsTC
ENST00000626498.2:c.*246-8_*246-7delinsTC	ENSP00000487527.1:n.*246-8_*246-7delinsTC
ENST00000626877.1:n.513-8_513-7delinsTC
NM_001109878.1:c.634-8_634-7delinsTC	NP_001103348.1:n.634-8_634-7delinsTC
NM_001109879.1:c.274-8_274-7delinsTC	NP_001103349.1:n.274-8_274-7delinsTC
NM_001303475.1:c.274-8_274-7delinsTC	NP_001290404.1:n.274-8_274-7delinsTC
NM_016954.2:c.634-8_634-7delinsTC	NP_058650.1:n.634-8_634-7delinsTC
XM_005262136.2:c.637-8_637-7delinsTC	XP_005262193.1:n.637-8_637-7delinsTC
XM_006724657.2:c.637-8_637-7delinsTC	XP_006724720.1:n.637-8_637-7delinsTC
XM_011530972.1:c.274-8_274-7delinsTC	XP_011529274.1:n.274-8_274-7delinsTC
NM_001109878.2:c.634-8_634-7delinsTC MANE Select	NP_001103348.1:n.634-8_634-7delinsTC
NM_001109879.2:c.274-8_274-7delinsTC	NP_001103349.1:n.274-8_274-7delinsTC