Canonical Allele Identifier: CA370308926
Gene: GATA4 HGNC NCBI

Linked Data

gnomAD v4: 8-11708433-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11708433A>G , CM000670.2:g.11708433A>G GRCh38
NC_000008.10:g.11565942A>G , CM000670.1:g.11565942A>G GRCh37
NC_000008.9:g.11603351A>G NCBI36
NG_008177.2:g.36515A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622443.3:c.121A>G ENSP00000482268.2:p.Thr41Ala
ENST00000532059.6:c.121A>G MANE Select ENSP00000435712.1:p.Thr41Ala
ENST00000335135.8:c.121A>G ENSP00000334458.4:p.Thr41Ala
ENST00000526716.5:c.-6+4129A>G ENSP00000435347.1:n.-6+4129A>G
ENST00000528027.1:c.121A>G ENSP00000432278.1:p.Thr41Ala
ENST00000528712.5:c.-6+7655A>G ENSP00000435043.1:n.-6+7655A>G
ENST00000532059.5:c.121A>G ENSP00000435712.1:p.Thr41Ala
ENST00000622443.2:c.120A>G ENSP00000482268.1:p.Pro40=
NM_001308093.1:c.121A>G NP_001295022.1:p.Thr41Ala
NM_001308094.1:c.-6+7655A>G NP_001295023.1:n.-6+7655A>G
NM_002052.3:c.121A>G NP_002043.2:p.Thr41Ala
NM_002052.4:c.121A>G NP_002043.2:p.Thr41Ala
XM_005272385.3:c.121A>G XP_005272442.1:p.Thr41Ala
XM_005272386.1:c.121A>G XP_005272443.1:p.Thr41Ala
XM_006716248.1:c.121A>G XP_006716311.1:p.Thr41Ala
XM_011543817.1:c.121A>G XP_011542119.1:p.Thr41Ala
XM_011543818.1:c.121A>G XP_011542120.1:p.Thr41Ala
XM_005272385.4:c.121A>G XP_005272442.1:p.Thr41Ala
XM_011543817.3:c.121A>G XP_011542119.1:p.Thr41Ala
XM_011543818.2:c.121A>G XP_011542120.1:p.Thr41Ala
XM_017013312.2:c.121A>G XP_016868801.1:p.Thr41Ala
NM_001308093.3:c.121A>G MANE Select NP_001295022.1:p.Thr41Ala
NM_001308094.2:c.-6+7655A>G NP_001295023.1:n.-6+7655A>G
NM_001374273.1:c.-3+4129A>G NP_001361202.1:n.-3+4129A>G
NM_001374274.1:c.-3+419A>G NP_001361203.1:n.-3+419A>G
NM_002052.5:c.121A>G NP_002043.2:p.Thr41Ala