Canonical Allele Identifier: CA370313028
Gene: GATA4 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11750174C>G , CM000670.2:g.11750174C>G GRCh38
NC_000008.10:g.11607683C>G , CM000670.1:g.11607683C>G GRCh37
NC_000008.9:g.11645092C>G NCBI36
NG_008177.2:g.78256C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622443.3:c.847C>G ENSP00000482268.2:p.Arg283Gly
ENST00000532059.6:c.850C>G MANE Select ENSP00000435712.1:p.Arg284Gly
ENST00000335135.8:c.847C>G ENSP00000334458.4:p.Arg283Gly
ENST00000526716.5:c.229C>G ENSP00000435347.1:p.Arg77Gly
ENST00000528712.5:c.229C>G ENSP00000435043.1:p.Arg77Gly
ENST00000532059.5:c.850C>G ENSP00000435712.1:p.Arg284Gly
ENST00000622443.2:c.844C>G ENSP00000482268.1:p.Arg282Gly
NM_001308093.1:c.850C>G NP_001295022.1:p.Arg284Gly
NM_001308094.1:c.229C>G NP_001295023.1:p.Arg77Gly
NM_002052.3:c.847C>G NP_002043.2:p.Arg283Gly
NM_002052.4:c.847C>G NP_002043.2:p.Arg283Gly
XM_005272385.3:c.850C>G XP_005272442.1:p.Arg284Gly
XM_005272386.1:c.850C>G XP_005272443.1:p.Arg284Gly
XM_006716248.1:c.850C>G XP_006716311.1:p.Arg284Gly
XM_011543817.1:c.850C>G XP_011542119.1:p.Arg284Gly
XM_011543818.1:c.850C>G XP_011542120.1:p.Arg284Gly
XM_005272385.4:c.850C>G XP_005272442.1:p.Arg284Gly
XM_011543817.3:c.850C>G XP_011542119.1:p.Arg284Gly
XM_011543818.2:c.850C>G XP_011542120.1:p.Arg284Gly
XM_017013312.2:c.850C>G XP_016868801.1:p.Arg284Gly
NM_001308093.3:c.850C>G MANE Select NP_001295022.1:p.Arg284Gly
NM_001308094.2:c.229C>G NP_001295023.1:p.Arg77Gly
NM_001374273.1:c.229C>G NP_001361202.1:p.Arg77Gly
NM_001374274.1:c.165+1089C>G NP_001361203.1:n.165+1089C>G
NM_002052.5:c.847C>G NP_002043.2:p.Arg283Gly