Canonical Allele Identifier: CA645611385
Gene: TBX22 HGNC NCBI

Linked Data

COSMIC: COSM388041

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.80026710_80026711delinsGA , CM000685.2:g.80026710_80026711delinsGA GRCh38
NC_000023.10:g.79282209_79282210delinsGA , CM000685.1:g.79282209_79282210delinsGA GRCh37
NC_000023.9:g.79168865_79168866delinsGA NCBI36
NG_008998.1:g.16955_16956delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000373296.8:c.640_641delinsGA MANE Select ENSP00000362393.3:p.Leu214Glu
ENST00000373294.8:c.640_641delinsGA ENSP00000362390.5:p.Leu214Glu
ENST00000373296.7:c.640_641delinsGA ENSP00000362393.3:p.Leu214Glu
ENST00000626498.2:c.*252_*253delinsGA ENSP00000487527.1:n.*252_*253delinsGA
ENST00000626877.1:n.519_520delinsGA
NM_001109878.1:c.640_641delinsGA NP_001103348.1:p.Leu214Glu
NM_001109879.1:c.280_281delinsGA NP_001103349.1:p.Leu94Glu
NM_001303475.1:c.280_281delinsGA NP_001290404.1:p.Leu94Glu
NM_016954.2:c.640_641delinsGA NP_058650.1:p.Leu214Glu
XM_005262136.2:c.643_644delinsGA XP_005262193.1:p.Leu215Glu
XM_006724657.2:c.643_644delinsGA XP_006724720.1:p.Leu215Glu
XM_011530972.1:c.280_281delinsGA XP_011529274.1:p.Leu94Glu
NM_001109878.2:c.640_641delinsGA MANE Select NP_001103348.1:p.Leu214Glu
NM_001109879.2:c.280_281delinsGA NP_001103349.1:p.Leu94Glu