Canonical Allele Identifier: CA645609783
Gene: TBX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19764991del , CM000684.2:g.19764991del GRCh38
NC_000022.10:g.19752514del , CM000684.1:g.19752514del GRCh37
NC_000022.9:g.18132514del NCBI36
NG_009229.1:g.13289del , LRG_226:g.13289del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700274.1:c.271del ENSP00000514909.1:p.Arg91AlafsTer?
ENST00000649276.2:c.745del MANE Select ENSP00000497003.1:p.Arg249AlafsTer?
ENST00000329705.11:c.718del ENSP00000331176.7:p.Arg240AlafsTer?
ENST00000332710.8:c.718del ENSP00000331791.4:p.Arg240AlafsTer?
ENST00000359500.7:c.718del ENSP00000352483.3:p.Arg240AlafsTer?
ENST00000621939.1:c.718del ENSP00000477982.1:p.Arg240AlafsTer?
NM_005992.1:c.718del NP_005983.1:p.Arg240AlafsTer?
NM_080646.1:c.718del NP_542377.1:p.Arg240AlafsTer?
NM_080647.1:c.718del , LRG_226t1:c.718del NP_542378.1:p.Arg240AlafsTer?
XM_006724312.1:c.718del XP_006724375.1:p.Arg240AlafsTer?
XM_011530351.1:c.745del XP_011528653.1:p.Arg249AlafsTer?
XM_006724312.2:c.718del XP_006724375.1:p.Arg240AlafsTer?
XM_017028925.1:c.868del XP_016884414.1:p.Arg290AlafsTer?
XM_017028926.1:c.718del XP_016884415.1:p.Arg240AlafsTer?
XM_017028927.1:c.19del XP_016884416.1:p.Arg7AlafsTer?
XM_017028928.1:c.868del XP_016884417.1:p.Arg290AlafsTer?
NM_001379200.1:c.745del MANE Select NP_001366129.1:p.Arg249AlafsTer?
NM_080646.2:c.718del NP_542377.1:p.Arg240AlafsTer?