Canonical Allele Identifier: CA347945
Gene: GATA4 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11708335C>A , CM000670.2:g.11708335C>A GRCh38
NC_000008.10:g.11565844C>A , CM000670.1:g.11565844C>A GRCh37
NC_000008.9:g.11603253C>A NCBI36
NG_008177.2:g.36417C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622443.3:c.23C>A ENSP00000482268.2:p.Ala8Asp
ENST00000532059.6:c.23C>A MANE Select ENSP00000435712.1:p.Ala8Asp
ENST00000335135.8:c.23C>A ENSP00000334458.4:p.Ala8Asp
ENST00000526716.5:c.-6+4031C>A ENSP00000435347.1:n.-6+4031C>A
ENST00000526974.1:c.23C>A ENSP00000473598.1:p.Ala8Asp
ENST00000528027.1:c.23C>A ENSP00000432278.1:p.Ala8Asp
ENST00000528712.5:c.-6+7557C>A ENSP00000435043.1:n.-6+7557C>A
ENST00000532059.5:c.23C>A ENSP00000435712.1:p.Ala8Asp
ENST00000532977.1:c.23C>A ENSP00000473671.1:p.Ala8Asp
ENST00000622443.2:c.22C>A ENSP00000482268.1:p.Pro8Thr
NM_001308093.1:c.23C>A NP_001295022.1:p.Ala8Asp
NM_001308094.1:c.-6+7557C>A NP_001295023.1:n.-6+7557C>A
NM_002052.3:c.23C>A NP_002043.2:p.Ala8Asp
NM_002052.4:c.23C>A NP_002043.2:p.Ala8Asp
XM_005272385.3:c.23C>A XP_005272442.1:p.Ala8Asp
XM_005272386.1:c.23C>A XP_005272443.1:p.Ala8Asp
XM_006716248.1:c.23C>A XP_006716311.1:p.Ala8Asp
XM_011543817.1:c.23C>A XP_011542119.1:p.Ala8Asp
XM_011543818.1:c.23C>A XP_011542120.1:p.Ala8Asp
XM_005272385.4:c.23C>A XP_005272442.1:p.Ala8Asp
XM_011543817.3:c.23C>A XP_011542119.1:p.Ala8Asp
XM_011543818.2:c.23C>A XP_011542120.1:p.Ala8Asp
XM_017013312.2:c.23C>A XP_016868801.1:p.Ala8Asp
NM_001308093.3:c.23C>A MANE Select NP_001295022.1:p.Ala8Asp
NM_001308094.2:c.-6+7557C>A NP_001295023.1:n.-6+7557C>A
NM_001374273.1:c.-3+4031C>A NP_001361202.1:n.-3+4031C>A
NM_001374274.1:c.-3+321C>A NP_001361203.1:n.-3+321C>A
NM_002052.5:c.23C>A NP_002043.2:p.Ala8Asp