Canonical Allele Identifier: CA1764051342
Gene: GATA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11703518_11703519delinsAG , CM000670.2:g.11703518_11703519delinsAG GRCh38
NC_000008.10:g.11561027_11561028delinsAG , CM000670.1:g.11561027_11561028delinsAG GRCh37
NC_000008.9:g.11598436_11598437delinsAG NCBI36
NG_008177.2:g.31600_31601delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000526974.1:c.-458+2740_-458+2741delinsAG ENSP00000473598.1:n.-458+2740_-458+2741delinsAG
ENST00000528712.5:c.-6+2740_-6+2741delinsAG ENSP00000435043.1:n.-6+2740_-6+2741delinsAG
ENST00000532977.1:c.-458+2740_-458+2741delinsAG ENSP00000473671.1:n.-458+2740_-458+2741delinsAG
NM_001308094.1:c.-6+2740_-6+2741delinsAG NP_001295023.1:n.-6+2740_-6+2741delinsAG
XM_005272386.1:c.-458+2740_-458+2741delinsAG XP_005272443.1:n.-458+2740_-458+2741delinsAG
XM_006716248.1:c.-458+2740_-458+2741delinsAG XP_006716311.1:n.-458+2740_-458+2741delinsAG
XM_011543817.1:c.-458+2740_-458+2741delinsAG XP_011542119.1:n.-458+2740_-458+2741delinsAG
XM_011543818.1:c.-458+3061_-458+3062delinsAG XP_011542120.1:n.-458+3061_-458+3062delinsAG
XM_011543817.3:c.-458+2740_-458+2741delinsAG XP_011542119.1:n.-458+2740_-458+2741delinsAG
XM_011543818.2:c.-458+3061_-458+3062delinsAG XP_011542120.1:n.-458+3061_-458+3062delinsAG
XM_017013312.2:c.-1244_-1243delinsAG XP_016868801.1:n.-1244_-1243delinsAG
NM_001308094.2:c.-6+2740_-6+2741delinsAG NP_001295023.1:n.-6+2740_-6+2741delinsAG