Canonical Allele Identifier: CA652201252
Gene: GATA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11758486dup , CM000670.2:g.11758486dup GRCh38
NC_000008.10:g.11615995dup , CM000670.1:g.11615995dup GRCh37
NC_000008.9:g.11653404dup NCBI36
NG_008177.2:g.86568dup

Transcript Alleles

HGVS Amino-acid change
ENST00000622443.3:c.*11dup ENSP00000482268.2:n.*11dup
ENST00000532059.6:c.*11dup MANE Select ENSP00000435712.1:n.*11dup
ENST00000335135.8:c.*11dup ENSP00000334458.4:n.*11dup
ENST00000526021.1:n.785dup
ENST00000528712.5:c.*11dup ENSP00000435043.1:n.*11dup
ENST00000532059.5:c.*11dup ENSP00000435712.1:n.*11dup
ENST00000622443.2:c.1337dup ENSP00000482268.1:n.1337dup
NM_001308093.1:c.*11dup NP_001295022.1:n.*11dup
NM_001308094.1:c.*11dup NP_001295023.1:n.*11dup
NM_002052.3:c.*11dup NP_002043.2:n.*11dup
NM_002052.4:c.*11dup NP_002043.2:n.*11dup
XM_005272385.3:c.*11dup XP_005272442.1:n.*11dup
XM_005272386.1:c.*11dup XP_005272443.1:n.*11dup
XM_006716248.1:c.*11dup XP_006716311.1:n.*11dup
XM_011543817.1:c.*11dup XP_011542119.1:n.*11dup
XM_011543818.1:c.*11dup XP_011542120.1:n.*11dup
XM_005272385.4:c.*11dup XP_005272442.1:n.*11dup
XM_011543817.3:c.*11dup XP_011542119.1:n.*11dup
XM_011543818.2:c.*11dup XP_011542120.1:n.*11dup
XM_017013312.2:c.*11dup XP_016868801.1:n.*11dup
NM_001308093.3:c.*11dup MANE Select NP_001295022.1:n.*11dup
NM_001308094.2:c.*11dup NP_001295023.1:n.*11dup
NM_001374273.1:c.*11dup NP_001361202.1:n.*11dup
NM_001374274.1:c.*11dup NP_001361203.1:n.*11dup
NM_002052.5:c.*11dup NP_002043.2:n.*11dup