Canonical Allele Identifier: CA2822025079

Gene: TBX22

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.80026864_80026865insCAACCAAACACACCCAAC , CM000685.2:g.80026864_80026865insCAACCAAACACACCCAAC	GRCh38
NC_000023.10:g.79282363_79282364insCAACCAAACACACCCAAC , CM000685.1:g.79282363_79282364insCAACCAAACACACCCAAC	GRCh37
NC_000023.9:g.79169019_79169020insCAACCAAACACACCCAAC	NCBI36
NG_008998.1:g.17109_17110insCAACCAAACACACCCAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373296.8:c.794_795insCAACCAAACACACCCAAC MANE Select	ENSP00000362393.3:p.Gln265delinsHisAsnGlnThrHisProThr
ENST00000373294.8:c.794_795insCAACCAAACACACCCAAC	ENSP00000362390.5:p.Gln265delinsHisAsnGlnThrHisProThr
ENST00000373296.7:c.794_795insCAACCAAACACACCCAAC	ENSP00000362393.3:p.Gln265delinsHisAsnGlnThrHisProThr
ENST00000626498.2:c.*406_*407insCAACCAAACACACCCAAC	ENSP00000487527.1:n.*406_*407insCAACCAAACACACCCAAC
ENST00000626877.1:n.673_674insCAACCAAACACACCCAAC
NM_001109878.1:c.794_795insCAACCAAACACACCCAAC	NP_001103348.1:p.Gln265delinsHisAsnGlnThrHisProThr
NM_001109879.1:c.434_435insCAACCAAACACACCCAAC	NP_001103349.1:p.Gln145delinsHisAsnGlnThrHisProThr
NM_001303475.1:c.434_435insCAACCAAACACACCCAAC	NP_001290404.1:p.Gln145delinsHisAsnGlnThrHisProThr
NM_016954.2:c.794_795insCAACCAAACACACCCAAC	NP_058650.1:p.Gln265delinsHisAsnGlnThrHisProThr
XM_005262136.2:c.797_798insCAACCAAACACACCCAAC	XP_005262193.1:p.Gln266delinsHisAsnGlnThrHisProThr
XM_006724657.2:c.797_798insCAACCAAACACACCCAAC	XP_006724720.1:p.Gln266delinsHisAsnGlnThrHisProThr
XM_011530972.1:c.434_435insCAACCAAACACACCCAAC	XP_011529274.1:p.Gln145delinsHisAsnGlnThrHisProThr
NM_001109878.2:c.794_795insCAACCAAACACACCCAAC MANE Select	NP_001103348.1:p.Gln265delinsHisAsnGlnThrHisProThr
NM_001109879.2:c.434_435insCAACCAAACACACCCAAC	NP_001103349.1:p.Gln145delinsHisAsnGlnThrHisProThr