Canonical Allele Identifier: CA2541363018
Gene: GATA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11703570G>T , CM000670.2:g.11703570G>T GRCh38
NC_000008.10:g.11561079G>T , CM000670.1:g.11561079G>T GRCh37
NC_000008.9:g.11598488G>T NCBI36
NG_008177.2:g.31652G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526974.1:c.-458+2792G>T ENSP00000473598.1:n.-458+2792G>T
ENST00000528712.5:c.-6+2792G>T ENSP00000435043.1:n.-6+2792G>T
ENST00000532977.1:c.-458+2792G>T ENSP00000473671.1:n.-458+2792G>T
NM_001308094.1:c.-6+2792G>T NP_001295023.1:n.-6+2792G>T
XM_005272386.1:c.-458+2792G>T XP_005272443.1:n.-458+2792G>T
XM_006716248.1:c.-458+2792G>T XP_006716311.1:n.-458+2792G>T
XM_011543817.1:c.-458+2792G>T XP_011542119.1:n.-458+2792G>T
XM_011543818.1:c.-458+3113G>T XP_011542120.1:n.-458+3113G>T
XM_011543817.3:c.-458+2792G>T XP_011542119.1:n.-458+2792G>T
XM_011543818.2:c.-458+3113G>T XP_011542120.1:n.-458+3113G>T
XM_017013312.2:c.-1192G>T XP_016868801.1:n.-1192G>T
NM_001308094.2:c.-6+2792G>T NP_001295023.1:n.-6+2792G>T