Canonical Allele Identifier: CA370313097

Gene: GATA4

Linked Data

• MyVariant Identifiers: chr8:g.11607714A>T (hg19) ; chr8:g.11750205A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11750205A>T , CM000670.2:g.11750205A>T	GRCh38
NC_000008.10:g.11607714A>T , CM000670.1:g.11607714A>T	GRCh37
NC_000008.9:g.11645123A>T	NCBI36
NG_008177.2:g.78287A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.878A>T	ENSP00000482268.2:p.Asn293Ile
ENST00000532059.6:c.881A>T MANE Select	ENSP00000435712.1:p.Asn294Ile
ENST00000335135.8:c.878A>T	ENSP00000334458.4:p.Asn293Ile
ENST00000526716.5:c.260A>T	ENSP00000435347.1:p.Asn87Ile
ENST00000528712.5:c.260A>T	ENSP00000435043.1:p.Asn87Ile
ENST00000532059.5:c.881A>T	ENSP00000435712.1:p.Asn294Ile
ENST00000622443.2:c.875A>T	ENSP00000482268.1:p.Asn292Ile
NM_001308093.1:c.881A>T	NP_001295022.1:p.Asn294Ile
NM_001308094.1:c.260A>T	NP_001295023.1:p.Asn87Ile
NM_002052.3:c.878A>T	NP_002043.2:p.Asn293Ile
NM_002052.4:c.878A>T	NP_002043.2:p.Asn293Ile
XM_005272385.3:c.881A>T	XP_005272442.1:p.Asn294Ile
XM_005272386.1:c.881A>T	XP_005272443.1:p.Asn294Ile
XM_006716248.1:c.881A>T	XP_006716311.1:p.Asn294Ile
XM_011543817.1:c.881A>T	XP_011542119.1:p.Asn294Ile
XM_011543818.1:c.881A>T	XP_011542120.1:p.Asn294Ile
XM_005272385.4:c.881A>T	XP_005272442.1:p.Asn294Ile
XM_011543817.3:c.881A>T	XP_011542119.1:p.Asn294Ile
XM_011543818.2:c.881A>T	XP_011542120.1:p.Asn294Ile
XM_017013312.2:c.881A>T	XP_016868801.1:p.Asn294Ile
NM_001308093.3:c.881A>T MANE Select	NP_001295022.1:p.Asn294Ile
NM_001308094.2:c.260A>T	NP_001295023.1:p.Asn87Ile
NM_001374273.1:c.260A>T	NP_001361202.1:p.Asn87Ile
NM_001374274.1:c.165+1120A>T	NP_001361203.1:n.165+1120A>T
NM_002052.5:c.878A>T	NP_002043.2:p.Asn293Ile