Canonical Allele Identifier: CA1764056591
Gene: GATA4 HGNC NCBI

Linked Data

dbSNP Id: rs1799983876
gnomAD v4: 8-11708274-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11708274G>A , CM000670.2:g.11708274G>A GRCh38
NC_000008.10:g.11565783G>A , CM000670.1:g.11565783G>A GRCh37
NC_000008.9:g.11603192G>A NCBI36
NG_008177.2:g.36356G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622443.3:c.-39G>A ENSP00000482268.2:n.-39G>A
ENST00000532059.6:c.-39G>A MANE Select ENSP00000435712.1:n.-39G>A
ENST00000335135.8:c.-39G>A ENSP00000334458.4:n.-39G>A
ENST00000526716.5:c.-6+3970G>A ENSP00000435347.1:n.-6+3970G>A
ENST00000526974.1:c.-39G>A ENSP00000473598.1:n.-39G>A
ENST00000528027.1:c.-39G>A ENSP00000432278.1:n.-39G>A
ENST00000528712.5:c.-6+7496G>A ENSP00000435043.1:n.-6+7496G>A
ENST00000532059.5:c.-39G>A ENSP00000435712.1:n.-39G>A
ENST00000532977.1:c.-39G>A ENSP00000473671.1:n.-39G>A
NM_001308093.1:c.-39G>A NP_001295022.1:n.-39G>A
NM_001308094.1:c.-6+7496G>A NP_001295023.1:n.-6+7496G>A
NM_002052.3:c.-39G>A NP_002043.2:n.-39G>A
NM_002052.4:c.-39G>A NP_002043.2:n.-39G>A
XM_005272385.3:c.-39G>A XP_005272442.1:n.-39G>A
XM_005272386.1:c.-39G>A XP_005272443.1:n.-39G>A
XM_006716248.1:c.-39G>A XP_006716311.1:n.-39G>A
XM_011543817.1:c.-39G>A XP_011542119.1:n.-39G>A
XM_011543818.1:c.-39G>A XP_011542120.1:n.-39G>A
XM_005272385.4:c.-39G>A XP_005272442.1:n.-39G>A
XM_011543817.3:c.-39G>A XP_011542119.1:n.-39G>A
XM_011543818.2:c.-39G>A XP_011542120.1:n.-39G>A
XM_017013312.2:c.-39G>A XP_016868801.1:n.-39G>A
NM_001308093.3:c.-39G>A MANE Select NP_001295022.1:n.-39G>A
NM_001308094.2:c.-6+7496G>A NP_001295023.1:n.-6+7496G>A
NM_001374273.1:c.-3+3970G>A NP_001361202.1:n.-3+3970G>A
NM_001374274.1:c.-3+260G>A NP_001361203.1:n.-3+260G>A
NM_002052.5:c.-39G>A NP_002043.2:n.-39G>A