Canonical Allele Identifier: CA172070048

Gene: GATA4

Linked Data

• dbSNP Id: rs757693844
• MyVariant Identifiers: chr8:g.11561057_11561059del (hg19) ; chr8:g.11703548_11703550del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11703550_11703552del , CM000670.2:g.11703550_11703552del	GRCh38
NC_000008.10:g.11561059_11561061del , CM000670.1:g.11561059_11561061del	GRCh37
NC_000008.9:g.11598468_11598470del	NCBI36
NG_008177.2:g.31632_31634del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526974.1:c.-458+2772_-458+2774del	ENSP00000473598.1:n.-458+2772_-458+2774del
ENST00000528712.5:c.-6+2772_-6+2774del	ENSP00000435043.1:n.-6+2772_-6+2774del
ENST00000532977.1:c.-458+2772_-458+2774del	ENSP00000473671.1:n.-458+2772_-458+2774del
NM_001308094.1:c.-6+2772_-6+2774del	NP_001295023.1:n.-6+2772_-6+2774del
XM_005272386.1:c.-458+2772_-458+2774del	XP_005272443.1:n.-458+2772_-458+2774del
XM_006716248.1:c.-458+2772_-458+2774del	XP_006716311.1:n.-458+2772_-458+2774del
XM_011543817.1:c.-458+2772_-458+2774del	XP_011542119.1:n.-458+2772_-458+2774del
XM_011543818.1:c.-458+3093_-458+3095del	XP_011542120.1:n.-458+3093_-458+3095del
XM_011543817.3:c.-458+2772_-458+2774del	XP_011542119.1:n.-458+2772_-458+2774del
XM_011543818.2:c.-458+3093_-458+3095del	XP_011542120.1:n.-458+3093_-458+3095del
XM_017013312.2:c.-1212_-1210del	XP_016868801.1:n.-1212_-1210del
NM_001308094.2:c.-6+2772_-6+2774del	NP_001295023.1:n.-6+2772_-6+2774del