Canonical Allele Identifier: CA1764074503
Gene: GATA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11758526T= , CM000670.2:g.11758526T= GRCh38
NC_000008.10:g.11616035T= , CM000670.1:g.11616035T= GRCh37
NC_000008.9:g.11653444T= NCBI36
NG_008177.2:g.86608T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622443.3:c.*51T= ENSP00000482268.2:n.*51T=
ENST00000532059.6:c.*51T= MANE Select ENSP00000435712.1:n.*51T=
ENST00000335135.8:c.*51T= ENSP00000334458.4:n.*51T=
ENST00000526021.1:n.825T=
ENST00000528712.5:c.*51T= ENSP00000435043.1:n.*51T=
ENST00000622443.2:c.1377T= ENSP00000482268.1:n.1377T=
NM_001308093.1:c.*51T= NP_001295022.1:n.*51T=
NM_001308094.1:c.*51T= NP_001295023.1:n.*51T=
NM_002052.3:c.*51T= NP_002043.2:n.*51T=
NM_002052.4:c.*51T= NP_002043.2:n.*51T=
XM_005272385.3:c.*51T= XP_005272442.1:n.*51T=
XM_005272386.1:c.*51T= XP_005272443.1:n.*51T=
XM_006716248.1:c.*51T= XP_006716311.1:n.*51T=
XM_011543817.1:c.*51T= XP_011542119.1:n.*51T=
XM_011543818.1:c.*51T= XP_011542120.1:n.*51T=
XM_005272385.4:c.*51T= XP_005272442.1:n.*51T=
XM_011543817.3:c.*51T= XP_011542119.1:n.*51T=
XM_011543818.2:c.*51T= XP_011542120.1:n.*51T=
XM_017013312.2:c.*51T= XP_016868801.1:n.*51T=
NM_001308093.3:c.*51T= MANE Select NP_001295022.1:n.*51T=
NM_001308094.2:c.*51T= NP_001295023.1:n.*51T=
NM_001374273.1:c.*51T= NP_001361202.1:n.*51T=
NM_001374274.1:c.*51T= NP_001361203.1:n.*51T=
NM_002052.5:c.*51T= NP_002043.2:n.*51T=