Canonical Allele Identifier: CA1764056969

Gene: GATA4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11708434C= , CM000670.2:g.11708434C=	GRCh38
NC_000008.10:g.11565943C= , CM000670.1:g.11565943C=	GRCh37
NC_000008.9:g.11603352C=	NCBI36
NG_008177.2:g.36516C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.122C=	ENSP00000482268.2:p.Thr41=
ENST00000532059.6:c.122C= MANE Select	ENSP00000435712.1:p.Thr41=
ENST00000335135.8:c.122C=	ENSP00000334458.4:p.Thr41=
ENST00000526716.5:c.-6+4130C=	ENSP00000435347.1:n.-6+4130C=
ENST00000528027.1:c.122C=	ENSP00000432278.1:p.Thr41=
ENST00000528712.5:c.-6+7656C=	ENSP00000435043.1:n.-6+7656C=
ENST00000532059.5:c.122C=	ENSP00000435712.1:p.Thr41=
ENST00000622443.2:c.121C=	ENSP00000482268.1:p.His41=
NM_001308093.1:c.122C=	NP_001295022.1:p.Thr41=
NM_001308094.1:c.-6+7656C=	NP_001295023.1:n.-6+7656C=
NM_002052.3:c.122C=	NP_002043.2:p.Thr41=
NM_002052.4:c.122C=	NP_002043.2:p.Thr41=
XM_005272385.3:c.122C=	XP_005272442.1:p.Thr41=
XM_005272386.1:c.122C=	XP_005272443.1:p.Thr41=
XM_006716248.1:c.122C=	XP_006716311.1:p.Thr41=
XM_011543817.1:c.122C=	XP_011542119.1:p.Thr41=
XM_011543818.1:c.122C=	XP_011542120.1:p.Thr41=
XM_005272385.4:c.122C=	XP_005272442.1:p.Thr41=
XM_011543817.3:c.122C=	XP_011542119.1:p.Thr41=
XM_011543818.2:c.122C=	XP_011542120.1:p.Thr41=
XM_017013312.2:c.122C=	XP_016868801.1:p.Thr41=
NM_001308093.3:c.122C= MANE Select	NP_001295022.1:p.Thr41=
NM_001308094.2:c.-6+7656C=	NP_001295023.1:n.-6+7656C=
NM_001374273.1:c.-3+4130C=	NP_001361202.1:n.-3+4130C=
NM_001374274.1:c.-3+420C=	NP_001361203.1:n.-3+420C=
NM_002052.5:c.122C=	NP_002043.2:p.Thr41=