Canonical Allele Identifier: CA1764056777

Gene: GATA4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11708351G= , CM000670.2:g.11708351G=	GRCh38
NC_000008.10:g.11565860G= , CM000670.1:g.11565860G=	GRCh37
NC_000008.9:g.11603269G=	NCBI36
NG_008177.2:g.36433G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.39G=	ENSP00000482268.2:p.Pro13=
ENST00000532059.6:c.39G= MANE Select	ENSP00000435712.1:p.Pro13=
ENST00000335135.8:c.39G=	ENSP00000334458.4:p.Pro13=
ENST00000526716.5:c.-6+4047G=	ENSP00000435347.1:n.-6+4047G=
ENST00000526974.1:c.39G=	ENSP00000473598.1:p.Pro13=
ENST00000528027.1:c.39G=	ENSP00000432278.1:p.Pro13=
ENST00000528712.5:c.-6+7573G=	ENSP00000435043.1:n.-6+7573G=
ENST00000532059.5:c.39G=	ENSP00000435712.1:p.Pro13=
ENST00000532977.1:c.39G=	ENSP00000473671.1:p.Pro13=
ENST00000622443.2:c.38G=	ENSP00000482268.1:p.Arg13=
NM_001308093.1:c.39G=	NP_001295022.1:p.Pro13=
NM_001308094.1:c.-6+7573G=	NP_001295023.1:n.-6+7573G=
NM_002052.3:c.39G=	NP_002043.2:p.Pro13=
NM_002052.4:c.39G=	NP_002043.2:p.Pro13=
XM_005272385.3:c.39G=	XP_005272442.1:p.Pro13=
XM_005272386.1:c.39G=	XP_005272443.1:p.Pro13=
XM_006716248.1:c.39G=	XP_006716311.1:p.Pro13=
XM_011543817.1:c.39G=	XP_011542119.1:p.Pro13=
XM_011543818.1:c.39G=	XP_011542120.1:p.Pro13=
XM_005272385.4:c.39G=	XP_005272442.1:p.Pro13=
XM_011543817.3:c.39G=	XP_011542119.1:p.Pro13=
XM_011543818.2:c.39G=	XP_011542120.1:p.Pro13=
XM_017013312.2:c.39G=	XP_016868801.1:p.Pro13=
NM_001308093.3:c.39G= MANE Select	NP_001295022.1:p.Pro13=
NM_001308094.2:c.-6+7573G=	NP_001295023.1:n.-6+7573G=
NM_001374273.1:c.-3+4047G=	NP_001361202.1:n.-3+4047G=
NM_001374274.1:c.-3+337G=	NP_001361203.1:n.-3+337G=
NM_002052.5:c.39G=	NP_002043.2:p.Pro13=