Canonical Allele Identifier: CA1764056597
Gene: GATA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11708275G= , CM000670.2:g.11708275G= GRCh38
NC_000008.10:g.11565784G= , CM000670.1:g.11565784G= GRCh37
NC_000008.9:g.11603193G= NCBI36
NG_008177.2:g.36357G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622443.3:c.-38G= ENSP00000482268.2:n.-38G=
ENST00000532059.6:c.-38G= MANE Select ENSP00000435712.1:n.-38G=
ENST00000335135.8:c.-38G= ENSP00000334458.4:n.-38G=
ENST00000526716.5:c.-6+3971G= ENSP00000435347.1:n.-6+3971G=
ENST00000526974.1:c.-38G= ENSP00000473598.1:n.-38G=
ENST00000528027.1:c.-38G= ENSP00000432278.1:n.-38G=
ENST00000528712.5:c.-6+7497G= ENSP00000435043.1:n.-6+7497G=
ENST00000532059.5:c.-38G= ENSP00000435712.1:n.-38G=
ENST00000532977.1:c.-38G= ENSP00000473671.1:n.-38G=
NM_001308093.1:c.-38G= NP_001295022.1:n.-38G=
NM_001308094.1:c.-6+7497G= NP_001295023.1:n.-6+7497G=
NM_002052.3:c.-38G= NP_002043.2:n.-38G=
NM_002052.4:c.-38G= NP_002043.2:n.-38G=
XM_005272385.3:c.-38G= XP_005272442.1:n.-38G=
XM_005272386.1:c.-38G= XP_005272443.1:n.-38G=
XM_006716248.1:c.-38G= XP_006716311.1:n.-38G=
XM_011543817.1:c.-38G= XP_011542119.1:n.-38G=
XM_011543818.1:c.-38G= XP_011542120.1:n.-38G=
XM_005272385.4:c.-38G= XP_005272442.1:n.-38G=
XM_011543817.3:c.-38G= XP_011542119.1:n.-38G=
XM_011543818.2:c.-38G= XP_011542120.1:n.-38G=
XM_017013312.2:c.-38G= XP_016868801.1:n.-38G=
NM_001308093.3:c.-38G= MANE Select NP_001295022.1:n.-38G=
NM_001308094.2:c.-6+7497G= NP_001295023.1:n.-6+7497G=
NM_001374273.1:c.-3+3971G= NP_001361202.1:n.-3+3971G=
NM_001374274.1:c.-3+261G= NP_001361203.1:n.-3+261G=
NM_002052.5:c.-38G= NP_002043.2:n.-38G=