Canonical Allele Identifier: CA1764057570

Gene: GATA4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11708799C= , CM000670.2:g.11708799C=	GRCh38
NC_000008.10:g.11566308C= , CM000670.1:g.11566308C=	GRCh37
NC_000008.9:g.11603717C=	NCBI36
NG_008177.2:g.36881C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000622443.3:c.487C=	ENSP00000482268.2:p.Pro163=
ENST00000532059.6:c.487C= MANE Select	ENSP00000435712.1:p.Pro163=
ENST00000335135.8:c.487C=	ENSP00000334458.4:p.Pro163=
ENST00000526716.5:c.-6+4495C=	ENSP00000435347.1:n.-6+4495C=
ENST00000528712.5:c.-6+8021C=	ENSP00000435043.1:n.-6+8021C=
ENST00000532059.5:c.487C=	ENSP00000435712.1:p.Pro163=
ENST00000622443.2:c.484C=	ENSP00000482268.1:p.Pro162=
NM_001308093.1:c.487C=	NP_001295022.1:p.Pro163=
NM_001308094.1:c.-6+8021C=	NP_001295023.1:n.-6+8021C=
NM_002052.3:c.487C=	NP_002043.2:p.Pro163=
NM_002052.4:c.487C=	NP_002043.2:p.Pro163=
XM_005272385.3:c.487C=	XP_005272442.1:p.Pro163=
XM_005272386.1:c.487C=	XP_005272443.1:p.Pro163=
XM_006716248.1:c.487C=	XP_006716311.1:p.Pro163=
XM_011543817.1:c.487C=	XP_011542119.1:p.Pro163=
XM_011543818.1:c.487C=	XP_011542120.1:p.Pro163=
XM_005272385.4:c.487C=	XP_005272442.1:p.Pro163=
XM_011543817.3:c.487C=	XP_011542119.1:p.Pro163=
XM_011543818.2:c.487C=	XP_011542120.1:p.Pro163=
XM_017013312.2:c.487C=	XP_016868801.1:p.Pro163=
NM_001308093.3:c.487C= MANE Select	NP_001295022.1:p.Pro163=
NM_001308094.2:c.-6+8021C=	NP_001295023.1:n.-6+8021C=
NM_001374273.1:c.-3+4495C=	NP_001361202.1:n.-3+4495C=
NM_001374274.1:c.-3+785C=	NP_001361203.1:n.-3+785C=
NM_002052.5:c.487C=	NP_002043.2:p.Pro163=