Canonical Allele Identifier: CA2655306565
Gene: TBX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19766777del , CM000684.2:g.19766777del GRCh38
NC_000022.10:g.19754300del , CM000684.1:g.19754300del GRCh37
NC_000022.9:g.18134300del NCBI36
NG_009229.1:g.15075del , LRG_226:g.15075del

Transcript Alleles

HGVS Amino-acid Change
ENST00000649276.2:c.1425del MANE Select ENSP00000497003.1:p.Ala476ProfsTer?
ENST00000329705.11:c.1009+775del ENSP00000331176.7:n.1009+775del
ENST00000332710.8:c.1398del ENSP00000331791.4:p.Ala467ProfsTer?
ENST00000359500.7:c.1009+775del ENSP00000352483.3:n.1009+775del
ENST00000621939.1:c.1009+775del ENSP00000477982.1:n.1009+775del
NM_005992.1:c.1009+775del NP_005983.1:n.1009+775del
NM_080646.1:c.1009+775del NP_542377.1:n.1009+775del
NM_080647.1:c.1398del , LRG_226t1:c.1398del NP_542378.1:p.Ala467ProfsTer?
XM_006724312.1:c.1398del XP_006724375.1:p.Ala467ProfsTer?
XM_011530351.1:c.1425del XP_011528653.1:p.Ala476ProfsTer?
XM_006724312.2:c.1398del XP_006724375.1:p.Ala467ProfsTer?
XM_017028925.1:c.1548del XP_016884414.1:p.Ala517ProfsTer?
XM_017028926.1:c.1398del XP_016884415.1:p.Ala467ProfsTer?
XM_017028927.1:c.753del XP_016884416.1:p.Ala252ProfsTer?
XM_017028928.1:c.1159+775del XP_016884417.1:n.1159+775del
NM_001379200.1:c.1425del MANE Select NP_001366129.1:p.Ala476ProfsTer?
NM_080646.2:c.1009+775del NP_542377.1:n.1009+775del