Canonical Allele Identifier: CA459313453

Gene: GATA4

Linked Data

• COSMIC: COSM3644451
• MyVariant Identifiers: chr8:g.11612578G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11755069G>A , CM000670.2:g.11755069G>A	GRCh38
NC_000008.10:g.11612578G>A , CM000670.1:g.11612578G>A	GRCh37
NC_000008.9:g.11649987G>A	NCBI36
NG_008177.2:g.83151G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000622443.3:c.933G>A	ENSP00000482268.2:p.Arg311=
ENST00000532059.6:c.936G>A MANE Select	ENSP00000435712.1:p.Arg312=
ENST00000335135.8:c.933G>A	ENSP00000334458.4:p.Arg311=
ENST00000526716.5:c.315G>A	ENSP00000435347.1:p.Arg105=
ENST00000528712.5:c.315G>A	ENSP00000435043.1:p.Arg105=
ENST00000532059.5:c.936G>A	ENSP00000435712.1:p.Arg312=
ENST00000622443.2:c.930G>A	ENSP00000482268.1:p.Arg310=
NM_001308093.1:c.936G>A	NP_001295022.1:p.Arg312=
NM_001308094.1:c.315G>A	NP_001295023.1:p.Arg105=
NM_002052.3:c.933G>A	NP_002043.2:p.Arg311=
NM_002052.4:c.933G>A	NP_002043.2:p.Arg311=
XM_005272385.3:c.936G>A	XP_005272442.1:p.Arg312=
XM_005272386.1:c.936G>A	XP_005272443.1:p.Arg312=
XM_006716248.1:c.936G>A	XP_006716311.1:p.Arg312=
XM_011543817.1:c.936G>A	XP_011542119.1:p.Arg312=
XM_011543818.1:c.936G>A	XP_011542120.1:p.Arg312=
XM_005272385.4:c.936G>A	XP_005272442.1:p.Arg312=
XM_011543817.3:c.936G>A	XP_011542119.1:p.Arg312=
XM_011543818.2:c.936G>A	XP_011542120.1:p.Arg312=
XM_017013312.2:c.936G>A	XP_016868801.1:p.Arg312=
NM_001308093.3:c.936G>A MANE Select	NP_001295022.1:p.Arg312=
NM_001308094.2:c.315G>A	NP_001295023.1:p.Arg105=
NM_001374273.1:c.315G>A	NP_001361202.1:p.Arg105=
NM_001374274.1:c.189G>A	NP_001361203.1:p.Arg63=
NM_002052.5:c.933G>A	NP_002043.2:p.Arg311=