Canonical Allele Identifier: CA1764056711

Gene: GATA4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11708333G= , CM000670.2:g.11708333G=	GRCh38
NC_000008.10:g.11565842G= , CM000670.1:g.11565842G=	GRCh37
NC_000008.9:g.11603251G=	NCBI36
NG_008177.2:g.36415G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.21G=	ENSP00000482268.2:p.Met7=
ENST00000532059.6:c.21G= MANE Select	ENSP00000435712.1:p.Met7=
ENST00000335135.8:c.21G=	ENSP00000334458.4:p.Met7=
ENST00000526716.5:c.-6+4029G=	ENSP00000435347.1:n.-6+4029G=
ENST00000526974.1:c.21G=	ENSP00000473598.1:p.Met7=
ENST00000528027.1:c.21G=	ENSP00000432278.1:p.Met7=
ENST00000528712.5:c.-6+7555G=	ENSP00000435043.1:n.-6+7555G=
ENST00000532059.5:c.21G=	ENSP00000435712.1:p.Met7=
ENST00000532977.1:c.21G=	ENSP00000473671.1:p.Met7=
ENST00000622443.2:c.20G=	ENSP00000482268.1:p.Trp7=
NM_001308093.1:c.21G=	NP_001295022.1:p.Met7=
NM_001308094.1:c.-6+7555G=	NP_001295023.1:n.-6+7555G=
NM_002052.3:c.21G=	NP_002043.2:p.Met7=
NM_002052.4:c.21G=	NP_002043.2:p.Met7=
XM_005272385.3:c.21G=	XP_005272442.1:p.Met7=
XM_005272386.1:c.21G=	XP_005272443.1:p.Met7=
XM_006716248.1:c.21G=	XP_006716311.1:p.Met7=
XM_011543817.1:c.21G=	XP_011542119.1:p.Met7=
XM_011543818.1:c.21G=	XP_011542120.1:p.Met7=
XM_005272385.4:c.21G=	XP_005272442.1:p.Met7=
XM_011543817.3:c.21G=	XP_011542119.1:p.Met7=
XM_011543818.2:c.21G=	XP_011542120.1:p.Met7=
XM_017013312.2:c.21G=	XP_016868801.1:p.Met7=
NM_001308093.3:c.21G= MANE Select	NP_001295022.1:p.Met7=
NM_001308094.2:c.-6+7555G=	NP_001295023.1:n.-6+7555G=
NM_001374273.1:c.-3+4029G=	NP_001361202.1:n.-3+4029G=
NM_001374274.1:c.-3+319G=	NP_001361203.1:n.-3+319G=
NM_002052.5:c.21G=	NP_002043.2:p.Met7=