Canonical Allele Identifier: CA1764072585

Gene: GATA4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11757077G= , CM000670.2:g.11757077G=	GRCh38
NC_000008.10:g.11614586G= , CM000670.1:g.11614586G=	GRCh37
NC_000008.9:g.11651995G=	NCBI36
NG_008177.2:g.85159G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000622443.3:c.1140G=	ENSP00000482268.2:p.Val380=
ENST00000532059.6:c.1143G= MANE Select	ENSP00000435712.1:p.Val381=
ENST00000335135.8:c.1140G=	ENSP00000334458.4:p.Val380=
ENST00000526021.1:n.585G=
ENST00000526716.5:c.522G=	ENSP00000435347.1:p.Val174=
ENST00000528712.5:c.522G=	ENSP00000435043.1:p.Val174=
ENST00000532059.5:c.1143G=	ENSP00000435712.1:p.Val381=
ENST00000622443.2:c.1137G=	ENSP00000482268.1:p.Val379=
NM_001308093.1:c.1143G=	NP_001295022.1:p.Val381=
NM_001308094.1:c.522G=	NP_001295023.1:p.Val174=
NM_002052.3:c.1140G=	NP_002043.2:p.Val380=
NM_002052.4:c.1140G=	NP_002043.2:p.Val380=
XM_005272385.3:c.1143G=	XP_005272442.1:p.Val381=
XM_005272386.1:c.1143G=	XP_005272443.1:p.Val381=
XM_006716248.1:c.1143G=	XP_006716311.1:p.Val381=
XM_011543817.1:c.1143G=	XP_011542119.1:p.Val381=
XM_011543818.1:c.1143G=	XP_011542120.1:p.Val381=
XM_005272385.4:c.1143G=	XP_005272442.1:p.Val381=
XM_011543817.3:c.1143G=	XP_011542119.1:p.Val381=
XM_011543818.2:c.1143G=	XP_011542120.1:p.Val381=
XM_017013312.2:c.1143G=	XP_016868801.1:p.Val381=
NM_001308093.3:c.1143G= MANE Select	NP_001295022.1:p.Val381=
NM_001308094.2:c.522G=	NP_001295023.1:p.Val174=
NM_001374273.1:c.522G=	NP_001361202.1:p.Val174=
NM_001374274.1:c.396G=	NP_001361203.1:p.Val132=
NM_002052.5:c.1140G=	NP_002043.2:p.Val380=