Canonical Allele Identifier: CA579774698

Gene: GATA4

Linked Data

• dbSNP Id: rs1189721776
• gnomAD v2: 8-11561021-G-GA
• gnomAD v3: 8-11703512-G-GA
• gnomAD v4: 8-11703512-G-GA
• MyVariant Identifiers: chr8:g.11561021_11561022insA (hg19) ; chr8:g.11703512_11703513insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11703518dup , CM000670.2:g.11703518dup	GRCh38
NC_000008.10:g.11561027dup , CM000670.1:g.11561027dup	GRCh37
NC_000008.9:g.11598436dup	NCBI36
NG_008177.2:g.31600dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526974.1:c.-458+2740dup	ENSP00000473598.1:n.-458+2740dup
ENST00000528712.5:c.-6+2740dup	ENSP00000435043.1:n.-6+2740dup
ENST00000532977.1:c.-458+2740dup	ENSP00000473671.1:n.-458+2740dup
NM_001308094.1:c.-6+2740dup	NP_001295023.1:n.-6+2740dup
XM_005272386.1:c.-458+2740dup	XP_005272443.1:n.-458+2740dup
XM_006716248.1:c.-458+2740dup	XP_006716311.1:n.-458+2740dup
XM_011543817.1:c.-458+2740dup	XP_011542119.1:n.-458+2740dup
XM_011543818.1:c.-458+3061dup	XP_011542120.1:n.-458+3061dup
XM_011543817.3:c.-458+2740dup	XP_011542119.1:n.-458+2740dup
XM_011543818.2:c.-458+3061dup	XP_011542120.1:n.-458+3061dup
XM_017013312.2:c.-1244dup	XP_016868801.1:n.-1244dup
NM_001308094.2:c.-6+2740dup	NP_001295023.1:n.-6+2740dup