Canonical Allele Identifier: CA2839374672
Gene: GATA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11758477dup , CM000670.2:g.11758477dup GRCh38
NC_000008.10:g.11615986dup , CM000670.1:g.11615986dup GRCh37
NC_000008.9:g.11653395dup NCBI36
NG_008177.2:g.86559dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000622443.3:c.*2dup ENSP00000482268.2:n.*2dup
ENST00000532059.6:c.*2dup MANE Select ENSP00000435712.1:n.*2dup
ENST00000335135.8:c.*2dup ENSP00000334458.4:n.*2dup
ENST00000526021.1:n.776dup
ENST00000528712.5:c.*2dup ENSP00000435043.1:n.*2dup
ENST00000532059.5:c.*2dup ENSP00000435712.1:n.*2dup
ENST00000622443.2:c.1328dup ENSP00000482268.1:n.1328dup
NM_001308093.1:c.*2dup NP_001295022.1:n.*2dup
NM_001308094.1:c.*2dup NP_001295023.1:n.*2dup
NM_002052.3:c.*2dup NP_002043.2:n.*2dup
NM_002052.4:c.*2dup NP_002043.2:n.*2dup
XM_005272385.3:c.*2dup XP_005272442.1:n.*2dup
XM_005272386.1:c.*2dup XP_005272443.1:n.*2dup
XM_006716248.1:c.*2dup XP_006716311.1:n.*2dup
XM_011543817.1:c.*2dup XP_011542119.1:n.*2dup
XM_011543818.1:c.*2dup XP_011542120.1:n.*2dup
XM_005272385.4:c.*2dup XP_005272442.1:n.*2dup
XM_011543817.3:c.*2dup XP_011542119.1:n.*2dup
XM_011543818.2:c.*2dup XP_011542120.1:n.*2dup
XM_017013312.2:c.*2dup XP_016868801.1:n.*2dup
NM_001308093.3:c.*2dup MANE Select NP_001295022.1:n.*2dup
NM_001308094.2:c.*2dup NP_001295023.1:n.*2dup
NM_001374273.1:c.*2dup NP_001361202.1:n.*2dup
NM_001374274.1:c.*2dup NP_001361203.1:n.*2dup
NM_002052.5:c.*2dup NP_002043.2:n.*2dup