Canonical Allele Identifier: CA2269031032
Gene: TBX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61456062_61456065delinsCAGG , CM000679.2:g.61456062_61456065delinsCAGG GRCh38
NC_000017.10:g.59533423_59533426delinsCAGG , CM000679.1:g.59533423_59533426delinsCAGG GRCh37
NC_000017.9:g.56888205_56888208delinsCAGG NCBI36
NG_008080.1:g.4617_4620delinsCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000644296.1:c.-3-426_-3-423delinsCAGG MANE Select ENSP00000495986.1:n.-3-426_-3-423delinsCAGG
ENST00000393853.8:c.-3-426_-3-423delinsCAGG ENSP00000377435.3:n.-3-426_-3-423delinsCAGG
ENST00000589003.5:c.-125-562_-125-559delinsCAGG ENSP00000467588.1:n.-125-562_-125-559delinsCAGG
XM_005257835.3:c.-3-426_-3-423delinsCAGG XP_005257892.2:n.-3-426_-3-423delinsCAGG
XM_005257837.2:c.-3-426_-3-423delinsCAGG XP_005257894.1:n.-3-426_-3-423delinsCAGG
XM_011525490.1:c.187-426_187-423delinsCAGG XP_011523792.1:n.187-426_187-423delinsCAGG
XM_011525491.1:c.187-426_187-423delinsCAGG XP_011523793.1:n.187-426_187-423delinsCAGG
XM_011525492.1:c.-3-426_-3-423delinsCAGG XP_011523794.1:n.-3-426_-3-423delinsCAGG
XM_011525493.1:c.-3-426_-3-423delinsCAGG XP_011523795.1:n.-3-426_-3-423delinsCAGG
XM_011525494.1:c.-4+327_-4+330delinsCAGG XP_011523796.1:n.-4+327_-4+330delinsCAGG
XM_011525495.1:c.187-426_187-423delinsCAGG XP_011523797.1:n.187-426_187-423delinsCAGG
NM_001321120.2:c.-3-426_-3-423delinsCAGG MANE Select NP_001308049.1:n.-3-426_-3-423delinsCAGG
XM_011525490.2:c.187-426_187-423delinsCAGG XP_011523792.1:n.187-426_187-423delinsCAGG
XM_011525491.2:c.187-426_187-423delinsCAGG XP_011523793.1:n.187-426_187-423delinsCAGG
XM_011525495.2:c.187-426_187-423delinsCAGG XP_011523797.1:n.187-426_187-423delinsCAGG