Canonical Allele Identifier: CA1764072508

Gene: GATA4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11757034C= , CM000670.2:g.11757034C=	GRCh38
NC_000008.10:g.11614543C= , CM000670.1:g.11614543C=	GRCh37
NC_000008.9:g.11651952C=	NCBI36
NG_008177.2:g.85116C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000622443.3:c.1097C=	ENSP00000482268.2:p.Thr366=
ENST00000532059.6:c.1100C= MANE Select	ENSP00000435712.1:p.Thr367=
ENST00000335135.8:c.1097C=	ENSP00000334458.4:p.Thr366=
ENST00000526021.1:n.542C=
ENST00000526716.5:c.479C=	ENSP00000435347.1:p.Thr160=
ENST00000528712.5:c.479C=	ENSP00000435043.1:p.Thr160=
ENST00000532059.5:c.1100C=	ENSP00000435712.1:p.Thr367=
ENST00000622443.2:c.1094C=	ENSP00000482268.1:p.Thr365=
NM_001308093.1:c.1100C=	NP_001295022.1:p.Thr367=
NM_001308094.1:c.479C=	NP_001295023.1:p.Thr160=
NM_002052.3:c.1097C=	NP_002043.2:p.Thr366=
NM_002052.4:c.1097C=	NP_002043.2:p.Thr366=
XM_005272385.3:c.1100C=	XP_005272442.1:p.Thr367=
XM_005272386.1:c.1100C=	XP_005272443.1:p.Thr367=
XM_006716248.1:c.1100C=	XP_006716311.1:p.Thr367=
XM_011543817.1:c.1100C=	XP_011542119.1:p.Thr367=
XM_011543818.1:c.1100C=	XP_011542120.1:p.Thr367=
XM_005272385.4:c.1100C=	XP_005272442.1:p.Thr367=
XM_011543817.3:c.1100C=	XP_011542119.1:p.Thr367=
XM_011543818.2:c.1100C=	XP_011542120.1:p.Thr367=
XM_017013312.2:c.1100C=	XP_016868801.1:p.Thr367=
NM_001308093.3:c.1100C= MANE Select	NP_001295022.1:p.Thr367=
NM_001308094.2:c.479C=	NP_001295023.1:p.Thr160=
NM_001374273.1:c.479C=	NP_001361202.1:p.Thr160=
NM_001374274.1:c.353C=	NP_001361203.1:p.Thr118=
NM_002052.5:c.1097C=	NP_002043.2:p.Thr366=