Canonical Allele Identifier: CA2064766856
Gene: TBX3 HGNC NCBI

Linked Data

dbSNP Id: rs1868631894
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674776_114674805del , CM000674.2:g.114674776_114674805del GRCh38
NC_000012.11:g.115112581_115112610del , CM000674.1:g.115112581_115112610del GRCh37
NC_000012.10:g.113596964_113596993del NCBI36
NG_008315.1:g.14368_14397del

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1078_1107del MANE Select ENSP00000257567.2:p.Glu360_Ala369del
ENST00000257566.7:c.1138_1167del ENSP00000257566.3:p.Glu380_Ala389del
ENST00000349155.6:c.1078_1107del ENSP00000257567.2:p.Glu360_Ala369del
ENST00000613550.1:c.1078_1107del ENSP00000480048.1:p.Glu360_Ala369del
NM_005996.3:c.1078_1107del NP_005987.3:p.Glu360_Ala369del
NM_016569.3:c.1138_1167del NP_057653.3:p.Glu380_Ala389del
NM_005996.4:c.1078_1107del MANE Select NP_005987.3:p.Glu360_Ala369del
NM_016569.4:c.1138_1167del NP_057653.3:p.Glu380_Ala389del
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