Canonical Allele Identifier: CA1764074441
Gene: GATA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11758480C= , CM000670.2:g.11758480C= GRCh38
NC_000008.10:g.11615989C= , CM000670.1:g.11615989C= GRCh37
NC_000008.9:g.11653398C= NCBI36
NG_008177.2:g.86562C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622443.3:c.*5C= ENSP00000482268.2:n.*5C=
ENST00000532059.6:c.*5C= MANE Select ENSP00000435712.1:n.*5C=
ENST00000335135.8:c.*5C= ENSP00000334458.4:n.*5C=
ENST00000526021.1:n.779C=
ENST00000528712.5:c.*5C= ENSP00000435043.1:n.*5C=
ENST00000532059.5:c.*5C= ENSP00000435712.1:n.*5C=
ENST00000622443.2:c.1331C= ENSP00000482268.1:n.1331C=
NM_001308093.1:c.*5C= NP_001295022.1:n.*5C=
NM_001308094.1:c.*5C= NP_001295023.1:n.*5C=
NM_002052.3:c.*5C= NP_002043.2:n.*5C=
NM_002052.4:c.*5C= NP_002043.2:n.*5C=
XM_005272385.3:c.*5C= XP_005272442.1:n.*5C=
XM_005272386.1:c.*5C= XP_005272443.1:n.*5C=
XM_006716248.1:c.*5C= XP_006716311.1:n.*5C=
XM_011543817.1:c.*5C= XP_011542119.1:n.*5C=
XM_011543818.1:c.*5C= XP_011542120.1:n.*5C=
XM_005272385.4:c.*5C= XP_005272442.1:n.*5C=
XM_011543817.3:c.*5C= XP_011542119.1:n.*5C=
XM_011543818.2:c.*5C= XP_011542120.1:n.*5C=
XM_017013312.2:c.*5C= XP_016868801.1:n.*5C=
NM_001308093.3:c.*5C= MANE Select NP_001295022.1:n.*5C=
NM_001308094.2:c.*5C= NP_001295023.1:n.*5C=
NM_001374273.1:c.*5C= NP_001361202.1:n.*5C=
NM_001374274.1:c.*5C= NP_001361203.1:n.*5C=
NM_002052.5:c.*5C= NP_002043.2:n.*5C=