Canonical Allele Identifier: CA846154937
Gene: GATA4 HGNC NCBI

Linked Data

dbSNP Id: rs1458846830
gnomAD v3: 8-11750083-C-A
gnomAD v4: 8-11750083-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11750083C>A , CM000670.2:g.11750083C>A GRCh38
NC_000008.10:g.11607592C>A , CM000670.1:g.11607592C>A GRCh37
NC_000008.9:g.11645001C>A NCBI36
NG_008177.2:g.78165C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000622443.3:c.784-28C>A ENSP00000482268.2:n.784-28C>A
ENST00000532059.6:c.787-28C>A MANE Select ENSP00000435712.1:n.787-28C>A
ENST00000335135.8:c.784-28C>A ENSP00000334458.4:n.784-28C>A
ENST00000526716.5:c.166-28C>A ENSP00000435347.1:n.166-28C>A
ENST00000528712.5:c.166-28C>A ENSP00000435043.1:n.166-28C>A
ENST00000532059.5:c.787-28C>A ENSP00000435712.1:n.787-28C>A
ENST00000622443.2:c.781-28C>A ENSP00000482268.1:n.781-28C>A
NM_001308093.1:c.787-28C>A NP_001295022.1:n.787-28C>A
NM_001308094.1:c.166-28C>A NP_001295023.1:n.166-28C>A
NM_002052.3:c.784-28C>A NP_002043.2:n.784-28C>A
NM_002052.4:c.784-28C>A NP_002043.2:n.784-28C>A
XM_005272385.3:c.787-28C>A XP_005272442.1:n.787-28C>A
XM_005272386.1:c.787-28C>A XP_005272443.1:n.787-28C>A
XM_006716248.1:c.787-28C>A XP_006716311.1:n.787-28C>A
XM_011543817.1:c.787-28C>A XP_011542119.1:n.787-28C>A
XM_011543818.1:c.787-28C>A XP_011542120.1:n.787-28C>A
XM_005272385.4:c.787-28C>A XP_005272442.1:n.787-28C>A
XM_011543817.3:c.787-28C>A XP_011542119.1:n.787-28C>A
XM_011543818.2:c.787-28C>A XP_011542120.1:n.787-28C>A
XM_017013312.2:c.787-28C>A XP_016868801.1:n.787-28C>A
NM_001308093.3:c.787-28C>A MANE Select NP_001295022.1:n.787-28C>A
NM_001308094.2:c.166-28C>A NP_001295023.1:n.166-28C>A
NM_001374273.1:c.166-28C>A NP_001361202.1:n.166-28C>A
NM_001374274.1:c.165+998C>A NP_001361203.1:n.165+998C>A
NM_002052.5:c.784-28C>A NP_002043.2:n.784-28C>A