Canonical Allele Identifier: CA459624795

Gene: GATA4

Linked Data

• dbSNP Id: rs1800015768
• gnomAD v4: 8-11708705-C-G
• MyVariant Identifiers: chr8:g.11566214C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11708705C>G , CM000670.2:g.11708705C>G	GRCh38
NC_000008.10:g.11566214C>G , CM000670.1:g.11566214C>G	GRCh37
NC_000008.9:g.11603623C>G	NCBI36
NG_008177.2:g.36787C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000622443.3:c.393C>G	ENSP00000482268.2:p.Ala131=
ENST00000532059.6:c.393C>G MANE Select	ENSP00000435712.1:p.Ala131=
ENST00000335135.8:c.393C>G	ENSP00000334458.4:p.Ala131=
ENST00000526716.5:c.-6+4401C>G	ENSP00000435347.1:n.-6+4401C>G
ENST00000528712.5:c.-6+7927C>G	ENSP00000435043.1:n.-6+7927C>G
ENST00000532059.5:c.393C>G	ENSP00000435712.1:p.Ala131=
ENST00000622443.2:c.390C>G	ENSP00000482268.1:p.Ala130=
NM_001308093.1:c.393C>G	NP_001295022.1:p.Ala131=
NM_001308094.1:c.-6+7927C>G	NP_001295023.1:n.-6+7927C>G
NM_002052.3:c.393C>G	NP_002043.2:p.Ala131=
NM_002052.4:c.393C>G	NP_002043.2:p.Ala131=
XM_005272385.3:c.393C>G	XP_005272442.1:p.Ala131=
XM_005272386.1:c.393C>G	XP_005272443.1:p.Ala131=
XM_006716248.1:c.393C>G	XP_006716311.1:p.Ala131=
XM_011543817.1:c.393C>G	XP_011542119.1:p.Ala131=
XM_011543818.1:c.393C>G	XP_011542120.1:p.Ala131=
XM_005272385.4:c.393C>G	XP_005272442.1:p.Ala131=
XM_011543817.3:c.393C>G	XP_011542119.1:p.Ala131=
XM_011543818.2:c.393C>G	XP_011542120.1:p.Ala131=
XM_017013312.2:c.393C>G	XP_016868801.1:p.Ala131=
NM_001308093.3:c.393C>G MANE Select	NP_001295022.1:p.Ala131=
NM_001308094.2:c.-6+7927C>G	NP_001295023.1:n.-6+7927C>G
NM_001374273.1:c.-3+4401C>G	NP_001361202.1:n.-3+4401C>G
NM_001374274.1:c.-3+691C>G	NP_001361203.1:n.-3+691C>G
NM_002052.5:c.393C>G	NP_002043.2:p.Ala131=