Canonical Allele Identifier: CA1764056658
Gene: GATA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11708310A= , CM000670.2:g.11708310A= GRCh38
NC_000008.10:g.11565819A= , CM000670.1:g.11565819A= GRCh37
NC_000008.9:g.11603228A= NCBI36
NG_008177.2:g.36392A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622443.3:c.-3A= ENSP00000482268.2:n.-3A=
ENST00000532059.6:c.-3A= MANE Select ENSP00000435712.1:n.-3A=
ENST00000335135.8:c.-3A= ENSP00000334458.4:n.-3A=
ENST00000526716.5:c.-6+4006A= ENSP00000435347.1:n.-6+4006A=
ENST00000526974.1:c.-3A= ENSP00000473598.1:n.-3A=
ENST00000528027.1:c.-3A= ENSP00000432278.1:n.-3A=
ENST00000528712.5:c.-6+7532A= ENSP00000435043.1:n.-6+7532A=
ENST00000532059.5:c.-3A= ENSP00000435712.1:n.-3A=
ENST00000532977.1:c.-3A= ENSP00000473671.1:n.-3A=
NM_001308093.1:c.-3A= NP_001295022.1:n.-3A=
NM_001308094.1:c.-6+7532A= NP_001295023.1:n.-6+7532A=
NM_002052.3:c.-3A= NP_002043.2:n.-3A=
NM_002052.4:c.-3A= NP_002043.2:n.-3A=
XM_005272385.3:c.-3A= XP_005272442.1:n.-3A=
XM_005272386.1:c.-3A= XP_005272443.1:n.-3A=
XM_006716248.1:c.-3A= XP_006716311.1:n.-3A=
XM_011543817.1:c.-3A= XP_011542119.1:n.-3A=
XM_011543818.1:c.-3A= XP_011542120.1:n.-3A=
XM_005272385.4:c.-3A= XP_005272442.1:n.-3A=
XM_011543817.3:c.-3A= XP_011542119.1:n.-3A=
XM_011543818.2:c.-3A= XP_011542120.1:n.-3A=
XM_017013312.2:c.-3A= XP_016868801.1:n.-3A=
NM_001308093.3:c.-3A= MANE Select NP_001295022.1:n.-3A=
NM_001308094.2:c.-6+7532A= NP_001295023.1:n.-6+7532A=
NM_001374273.1:c.-3+4006A= NP_001361202.1:n.-3+4006A=
NM_001374274.1:c.-3+296A= NP_001361203.1:n.-3+296A=
NM_002052.5:c.-3A= NP_002043.2:n.-3A=