Canonical Allele Identifier: CA370308540

Gene: GATA4

Linked Data

• dbSNP Id: rs1585594672
• gnomAD v4: 8-11708344-A-G
• MyVariant Identifiers: chr8:g.11565853A>G (hg19) ; chr8:g.11708344A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11708344A>G , CM000670.2:g.11708344A>G	GRCh38
NC_000008.10:g.11565853A>G , CM000670.1:g.11565853A>G	GRCh37
NC_000008.9:g.11603262A>G	NCBI36
NG_008177.2:g.36426A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.32A>G	ENSP00000482268.2:p.His11Arg
ENST00000532059.6:c.32A>G MANE Select	ENSP00000435712.1:p.His11Arg
ENST00000335135.8:c.32A>G	ENSP00000334458.4:p.His11Arg
ENST00000526716.5:c.-6+4040A>G	ENSP00000435347.1:n.-6+4040A>G
ENST00000526974.1:c.32A>G	ENSP00000473598.1:p.His11Arg
ENST00000528027.1:c.32A>G	ENSP00000432278.1:p.His11Arg
ENST00000528712.5:c.-6+7566A>G	ENSP00000435043.1:n.-6+7566A>G
ENST00000532059.5:c.32A>G	ENSP00000435712.1:p.His11Arg
ENST00000532977.1:c.32A>G	ENSP00000473671.1:p.His11Arg
ENST00000622443.2:c.31A>G	ENSP00000482268.1:p.Thr11Ala
NM_001308093.1:c.32A>G	NP_001295022.1:p.His11Arg
NM_001308094.1:c.-6+7566A>G	NP_001295023.1:n.-6+7566A>G
NM_002052.3:c.32A>G	NP_002043.2:p.His11Arg
NM_002052.4:c.32A>G	NP_002043.2:p.His11Arg
XM_005272385.3:c.32A>G	XP_005272442.1:p.His11Arg
XM_005272386.1:c.32A>G	XP_005272443.1:p.His11Arg
XM_006716248.1:c.32A>G	XP_006716311.1:p.His11Arg
XM_011543817.1:c.32A>G	XP_011542119.1:p.His11Arg
XM_011543818.1:c.32A>G	XP_011542120.1:p.His11Arg
XM_005272385.4:c.32A>G	XP_005272442.1:p.His11Arg
XM_011543817.3:c.32A>G	XP_011542119.1:p.His11Arg
XM_011543818.2:c.32A>G	XP_011542120.1:p.His11Arg
XM_017013312.2:c.32A>G	XP_016868801.1:p.His11Arg
NM_001308093.3:c.32A>G MANE Select	NP_001295022.1:p.His11Arg
NM_001308094.2:c.-6+7566A>G	NP_001295023.1:n.-6+7566A>G
NM_001374273.1:c.-3+4040A>G	NP_001361202.1:n.-3+4040A>G
NM_001374274.1:c.-3+330A>G	NP_001361203.1:n.-3+330A>G
NM_002052.5:c.32A>G	NP_002043.2:p.His11Arg