Canonical Allele Identifier: CA1764079823

Gene: GATA4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11749073T= , CM000670.2:g.11749073T=	GRCh38
NC_000008.10:g.11606582T= , CM000670.1:g.11606582T=	GRCh37
NC_000008.9:g.11643991T=	NCBI36
NG_008177.2:g.77155T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.771T=	ENSP00000482268.2:p.Pro257=
ENST00000532059.6:c.774T= MANE Select	ENSP00000435712.1:p.Pro258=
ENST00000335135.8:c.771T=	ENSP00000334458.4:p.Pro257=
ENST00000526716.5:c.153T=	ENSP00000435347.1:p.Pro51=
ENST00000528712.5:c.153T=	ENSP00000435043.1:p.Pro51=
ENST00000532059.5:c.774T=	ENSP00000435712.1:p.Pro258=
ENST00000622443.2:c.768T=	ENSP00000482268.1:p.Pro256=
NM_001308093.1:c.774T=	NP_001295022.1:p.Pro258=
NM_001308094.1:c.153T=	NP_001295023.1:p.Pro51=
NM_002052.3:c.771T=	NP_002043.2:p.Pro257=
NM_002052.4:c.771T=	NP_002043.2:p.Pro257=
XM_005272385.3:c.774T=	XP_005272442.1:p.Pro258=
XM_005272386.1:c.774T=	XP_005272443.1:p.Pro258=
XM_006716248.1:c.774T=	XP_006716311.1:p.Pro258=
XM_011543817.1:c.774T=	XP_011542119.1:p.Pro258=
XM_011543818.1:c.774T=	XP_011542120.1:p.Pro258=
XM_005272385.4:c.774T=	XP_005272442.1:p.Pro258=
XM_011543817.3:c.774T=	XP_011542119.1:p.Pro258=
XM_011543818.2:c.774T=	XP_011542120.1:p.Pro258=
XM_017013312.2:c.774T=	XP_016868801.1:p.Pro258=
NM_001308093.3:c.774T= MANE Select	NP_001295022.1:p.Pro258=
NM_001308094.2:c.153T=	NP_001295023.1:p.Pro51=
NM_001374273.1:c.153T=	NP_001361202.1:p.Pro51=
NM_001374274.1:c.153T=	NP_001361203.1:p.Pro51=
NM_002052.5:c.771T=	NP_002043.2:p.Pro257=