Canonical Allele Identifier: CA1764081015
Gene: GATA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11750069A= , CM000670.2:g.11750069A= GRCh38
NC_000008.10:g.11607578A= , CM000670.1:g.11607578A= GRCh37
NC_000008.9:g.11644987A= NCBI36
NG_008177.2:g.78151A=

Transcript Alleles

HGVS Amino-acid change
ENST00000622443.3:c.784-42A= ENSP00000482268.2:n.784-42A=
ENST00000532059.6:c.787-42A= MANE Select ENSP00000435712.1:n.787-42A=
ENST00000335135.8:c.784-42A= ENSP00000334458.4:n.784-42A=
ENST00000526716.5:c.166-42A= ENSP00000435347.1:n.166-42A=
ENST00000528712.5:c.166-42A= ENSP00000435043.1:n.166-42A=
ENST00000532059.5:c.787-42A= ENSP00000435712.1:n.787-42A=
ENST00000622443.2:c.781-42A= ENSP00000482268.1:n.781-42A=
NM_001308093.1:c.787-42A= NP_001295022.1:n.787-42A=
NM_001308094.1:c.166-42A= NP_001295023.1:n.166-42A=
NM_002052.3:c.784-42A= NP_002043.2:n.784-42A=
NM_002052.4:c.784-42A= NP_002043.2:n.784-42A=
XM_005272385.3:c.787-42A= XP_005272442.1:n.787-42A=
XM_005272386.1:c.787-42A= XP_005272443.1:n.787-42A=
XM_006716248.1:c.787-42A= XP_006716311.1:n.787-42A=
XM_011543817.1:c.787-42A= XP_011542119.1:n.787-42A=
XM_011543818.1:c.787-42A= XP_011542120.1:n.787-42A=
XM_005272385.4:c.787-42A= XP_005272442.1:n.787-42A=
XM_011543817.3:c.787-42A= XP_011542119.1:n.787-42A=
XM_011543818.2:c.787-42A= XP_011542120.1:n.787-42A=
XM_017013312.2:c.787-42A= XP_016868801.1:n.787-42A=
NM_001308093.3:c.787-42A= MANE Select NP_001295022.1:n.787-42A=
NM_001308094.2:c.166-42A= NP_001295023.1:n.166-42A=
NM_001374273.1:c.166-42A= NP_001361202.1:n.166-42A=
NM_001374274.1:c.165+984A= NP_001361203.1:n.165+984A=
NM_002052.5:c.784-42A= NP_002043.2:n.784-42A=