Canonical Allele Identifier: CA1764072521
Gene: GATA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11757038G= , CM000670.2:g.11757038G= GRCh38
NC_000008.10:g.11614547G= , CM000670.1:g.11614547G= GRCh37
NC_000008.9:g.11651956G= NCBI36
NG_008177.2:g.85120G=

Transcript Alleles

HGVS Amino-acid change
ENST00000622443.3:c.1101G= ENSP00000482268.2:p.Glu367=
ENST00000532059.6:c.1104G= MANE Select ENSP00000435712.1:p.Glu368=
ENST00000335135.8:c.1101G= ENSP00000334458.4:p.Glu367=
ENST00000526021.1:n.546G=
ENST00000526716.5:c.483G= ENSP00000435347.1:p.Glu161=
ENST00000528712.5:c.483G= ENSP00000435043.1:p.Glu161=
ENST00000532059.5:c.1104G= ENSP00000435712.1:p.Glu368=
ENST00000622443.2:c.1098G= ENSP00000482268.1:p.Glu366=
NM_001308093.1:c.1104G= NP_001295022.1:p.Glu368=
NM_001308094.1:c.483G= NP_001295023.1:p.Glu161=
NM_002052.3:c.1101G= NP_002043.2:p.Glu367=
NM_002052.4:c.1101G= NP_002043.2:p.Glu367=
XM_005272385.3:c.1104G= XP_005272442.1:p.Glu368=
XM_005272386.1:c.1104G= XP_005272443.1:p.Glu368=
XM_006716248.1:c.1104G= XP_006716311.1:p.Glu368=
XM_011543817.1:c.1104G= XP_011542119.1:p.Glu368=
XM_011543818.1:c.1104G= XP_011542120.1:p.Glu368=
XM_005272385.4:c.1104G= XP_005272442.1:p.Glu368=
XM_011543817.3:c.1104G= XP_011542119.1:p.Glu368=
XM_011543818.2:c.1104G= XP_011542120.1:p.Glu368=
XM_017013312.2:c.1104G= XP_016868801.1:p.Glu368=
NM_001308093.3:c.1104G= MANE Select NP_001295022.1:p.Glu368=
NM_001308094.2:c.483G= NP_001295023.1:p.Glu161=
NM_001374273.1:c.483G= NP_001361202.1:p.Glu161=
NM_001374274.1:c.357G= NP_001361203.1:p.Glu119=
NM_002052.5:c.1101G= NP_002043.2:p.Glu367=