Canonical Allele Identifier: CA1764074118

Gene: GATA4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11758320C= , CM000670.2:g.11758320C=	GRCh38
NC_000008.10:g.11615829C= , CM000670.1:g.11615829C=	GRCh37
NC_000008.9:g.11653238C=	NCBI36
NG_008177.2:g.86402C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.1174C=	ENSP00000482268.2:p.His392=
ENST00000532059.6:c.1177C= MANE Select	ENSP00000435712.1:p.His393=
ENST00000335135.8:c.1174C=	ENSP00000334458.4:p.His392=
ENST00000526021.1:n.619C=
ENST00000528712.5:c.556C=	ENSP00000435043.1:p.His186=
ENST00000532059.5:c.1177C=	ENSP00000435712.1:p.His393=
ENST00000622443.2:c.1171C=	ENSP00000482268.1:p.His391=
NM_001308093.1:c.1177C=	NP_001295022.1:p.His393=
NM_001308094.1:c.556C=	NP_001295023.1:p.His186=
NM_002052.3:c.1174C=	NP_002043.2:p.His392=
NM_002052.4:c.1174C=	NP_002043.2:p.His392=
XM_005272385.3:c.1177C=	XP_005272442.1:p.His393=
XM_005272386.1:c.1177C=	XP_005272443.1:p.His393=
XM_006716248.1:c.1177C=	XP_006716311.1:p.His393=
XM_011543817.1:c.1177C=	XP_011542119.1:p.His393=
XM_011543818.1:c.1177C=	XP_011542120.1:p.His393=
XM_005272385.4:c.1177C=	XP_005272442.1:p.His393=
XM_011543817.3:c.1177C=	XP_011542119.1:p.His393=
XM_011543818.2:c.1177C=	XP_011542120.1:p.His393=
XM_017013312.2:c.1177C=	XP_016868801.1:p.His393=
NM_001308093.3:c.1177C= MANE Select	NP_001295022.1:p.His393=
NM_001308094.2:c.556C=	NP_001295023.1:p.His186=
NM_001374273.1:c.556C=	NP_001361202.1:p.His186=
NM_001374274.1:c.430C=	NP_001361203.1:p.His144=
NM_002052.5:c.1174C=	NP_002043.2:p.His392=