Canonical Allele Identifier: CA1764056908
Gene: GATA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11708395A= , CM000670.2:g.11708395A= GRCh38
NC_000008.10:g.11565904A= , CM000670.1:g.11565904A= GRCh37
NC_000008.9:g.11603313A= NCBI36
NG_008177.2:g.36477A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622443.3:c.83A= ENSP00000482268.2:p.His28=
ENST00000532059.6:c.83A= MANE Select ENSP00000435712.1:p.His28=
ENST00000335135.8:c.83A= ENSP00000334458.4:p.His28=
ENST00000526716.5:c.-6+4091A= ENSP00000435347.1:n.-6+4091A=
ENST00000528027.1:c.83A= ENSP00000432278.1:p.His28=
ENST00000528712.5:c.-6+7617A= ENSP00000435043.1:n.-6+7617A=
ENST00000532059.5:c.83A= ENSP00000435712.1:p.His28=
ENST00000622443.2:c.82A= ENSP00000482268.1:p.Thr28=
NM_001308093.1:c.83A= NP_001295022.1:p.His28=
NM_001308094.1:c.-6+7617A= NP_001295023.1:n.-6+7617A=
NM_002052.3:c.83A= NP_002043.2:p.His28=
NM_002052.4:c.83A= NP_002043.2:p.His28=
XM_005272385.3:c.83A= XP_005272442.1:p.His28=
XM_005272386.1:c.83A= XP_005272443.1:p.His28=
XM_006716248.1:c.83A= XP_006716311.1:p.His28=
XM_011543817.1:c.83A= XP_011542119.1:p.His28=
XM_011543818.1:c.83A= XP_011542120.1:p.His28=
XM_005272385.4:c.83A= XP_005272442.1:p.His28=
XM_011543817.3:c.83A= XP_011542119.1:p.His28=
XM_011543818.2:c.83A= XP_011542120.1:p.His28=
XM_017013312.2:c.83A= XP_016868801.1:p.His28=
NM_001308093.3:c.83A= MANE Select NP_001295022.1:p.His28=
NM_001308094.2:c.-6+7617A= NP_001295023.1:n.-6+7617A=
NM_001374273.1:c.-3+4091A= NP_001361202.1:n.-3+4091A=
NM_001374274.1:c.-3+381A= NP_001361203.1:n.-3+381A=
NM_002052.5:c.83A= NP_002043.2:p.His28=