Canonical Allele Identifier: CA2686162603
Gene: GATA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11708614del , CM000670.2:g.11708614del GRCh38
NC_000008.10:g.11566123del , CM000670.1:g.11566123del GRCh37
NC_000008.9:g.11603532del NCBI36
NG_008177.2:g.36696del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622443.3:c.302del ENSP00000482268.2:p.Pro101ArgfsTer?
ENST00000532059.6:c.302del MANE Select ENSP00000435712.1:p.Pro101ArgfsTer?
ENST00000335135.8:c.302del ENSP00000334458.4:p.Pro101ArgfsTer?
ENST00000526716.5:c.-6+4310del ENSP00000435347.1:n.-6+4310del
ENST00000528027.1:c.302del ENSP00000432278.1:p.Pro101ArgfsTer?
ENST00000528712.5:c.-6+7836del ENSP00000435043.1:n.-6+7836del
ENST00000532059.5:c.302del ENSP00000435712.1:p.Pro101ArgfsTer?
ENST00000622443.2:c.299del ENSP00000482268.1:p.Pro100ArgfsTer?
NM_001308093.1:c.302del NP_001295022.1:p.Pro101ArgfsTer?
NM_001308094.1:c.-6+7836del NP_001295023.1:n.-6+7836del
NM_002052.3:c.302del NP_002043.2:p.Pro101ArgfsTer?
NM_002052.4:c.302del NP_002043.2:p.Pro101ArgfsTer?
XM_005272385.3:c.302del XP_005272442.1:p.Pro101ArgfsTer?
XM_005272386.1:c.302del XP_005272443.1:p.Pro101ArgfsTer?
XM_006716248.1:c.302del XP_006716311.1:p.Pro101ArgfsTer?
XM_011543817.1:c.302del XP_011542119.1:p.Pro101ArgfsTer?
XM_011543818.1:c.302del XP_011542120.1:p.Pro101ArgfsTer?
XM_005272385.4:c.302del XP_005272442.1:p.Pro101ArgfsTer?
XM_011543817.3:c.302del XP_011542119.1:p.Pro101ArgfsTer?
XM_011543818.2:c.302del XP_011542120.1:p.Pro101ArgfsTer?
XM_017013312.2:c.302del XP_016868801.1:p.Pro101ArgfsTer?
NM_001308093.3:c.302del MANE Select NP_001295022.1:p.Pro101ArgfsTer?
NM_001308094.2:c.-6+7836del NP_001295023.1:n.-6+7836del
NM_001374273.1:c.-3+4310del NP_001361202.1:n.-3+4310del
NM_001374274.1:c.-3+600del NP_001361203.1:n.-3+600del
NM_002052.5:c.302del NP_002043.2:p.Pro101ArgfsTer?