Canonical Allele Identifier: CA2818396737
Gene: TBX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19766703_19766704insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT , CM000684.2:g.19766703_19766704insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT GRCh38
NC_000022.10:g.19754226_19754227insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT , CM000684.1:g.19754226_19754227insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT GRCh37
NC_000022.9:g.18134226_18134227insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT NCBI36
NG_009229.1:g.15001_15002insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT , LRG_226:g.15001_15002insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000649276.2:c.1351_1352insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT MANE Select ENSP00000497003.1:p.Arg451GlnfsTer19
ENST00000329705.11:c.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT ENSP00000331176.7:n.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCG...
ENST00000332710.8:c.1324_1325insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT ENSP00000331791.4:p.Arg442GlnfsTer19
ENST00000359500.7:c.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT ENSP00000352483.3:n.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCG...
ENST00000621939.1:c.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT ENSP00000477982.1:n.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCG...
NM_005992.1:c.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT NP_005983.1:n.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCGAGAGCC...
NM_080646.1:c.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT NP_542377.1:n.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCGAGAGCC...
NM_080647.1:c.1324_1325insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT , LRG_226t1:c.1324_1325insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT NP_542378.1:p.Arg442GlnfsTer19
XM_006724312.1:c.1324_1325insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT XP_006724375.1:p.Arg442GlnfsTer19
XM_011530351.1:c.1351_1352insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT XP_011528653.1:p.Arg451GlnfsTer19
XM_006724312.2:c.1324_1325insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT XP_006724375.1:p.Arg442GlnfsTer19
XM_017028925.1:c.1474_1475insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT XP_016884414.1:p.Arg492GlnfsTer19
XM_017028926.1:c.1324_1325insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT XP_016884415.1:p.Arg442GlnfsTer19
XM_017028927.1:c.679_680insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT XP_016884416.1:p.Arg227GlnfsTer19
XM_017028928.1:c.1159+701_1159+702insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT XP_016884417.1:n.1159+701_1159+702insAGTTGCAGTGTAGACAGCCCGAGA...
NM_001379200.1:c.1351_1352insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT MANE Select NP_001366129.1:p.Arg451GlnfsTer19
NM_080646.2:c.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGATACATGTAGATACT NP_542377.1:n.1009+701_1009+702insAGTTGCAGTGTAGACAGCCCGAGAGCC...