Canonical Allele Identifier: CA2064790013
Gene: TBX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114670411_114670415delinsAATAT , CM000674.2:g.114670411_114670415delinsAATAT GRCh38
NC_000012.11:g.115108216_115108220delinsAATAT , CM000674.1:g.115108216_115108220delinsAATAT GRCh37
NC_000012.10:g.113592599_113592603delinsAATAT NCBI36
NG_008315.1:g.18750_18754delinsATATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.*1426_*1430delinsATATT MANE Select ENSP00000257567.2:n.*1426_*1430delinsATATT
ENST00000257566.7:c.*1426_*1430delinsATATT ENSP00000257566.3:n.*1426_*1430delinsATATT
ENST00000349155.6:c.*1426_*1430delinsATATT ENSP00000257567.2:n.*1426_*1430delinsATATT
NM_005996.3:c.*1426_*1430delinsATATT NP_005987.3:n.*1426_*1430delinsATATT
NM_016569.3:c.*1426_*1430delinsATATT NP_057653.3:n.*1426_*1430delinsATATT
NM_005996.4:c.*1426_*1430delinsATATT MANE Select NP_005987.3:n.*1426_*1430delinsATATT
NM_016569.4:c.*1426_*1430delinsATATT NP_057653.3:n.*1426_*1430delinsATATT