Canonical Allele Identifier: CA2686137591

Gene: GATA4

Linked Data

• gnomAD v4: 8-11758636-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11758636C>G , CM000670.2:g.11758636C>G	GRCh38
NC_000008.10:g.11616145C>G , CM000670.1:g.11616145C>G	GRCh37
NC_000008.9:g.11653554C>G	NCBI36
NG_008177.2:g.86718C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.*161C>G	ENSP00000482268.2:n.*161C>G
ENST00000532059.6:c.*161C>G MANE Select	ENSP00000435712.1:n.*161C>G
ENST00000335135.8:c.*161C>G	ENSP00000334458.4:n.*161C>G
ENST00000526021.1:n.935C>G
ENST00000528712.5:c.*161C>G	ENSP00000435043.1:n.*161C>G
ENST00000622443.2:c.1487C>G	ENSP00000482268.1:n.1487C>G
NM_001308093.1:c.*161C>G	NP_001295022.1:n.*161C>G
NM_001308094.1:c.*161C>G	NP_001295023.1:n.*161C>G
NM_002052.3:c.*161C>G	NP_002043.2:n.*161C>G
NM_002052.4:c.*161C>G	NP_002043.2:n.*161C>G
XM_005272385.3:c.*161C>G	XP_005272442.1:n.*161C>G
XM_005272386.1:c.*161C>G	XP_005272443.1:n.*161C>G
XM_006716248.1:c.*161C>G	XP_006716311.1:n.*161C>G
XM_011543817.1:c.*161C>G	XP_011542119.1:n.*161C>G
XM_011543818.1:c.*161C>G	XP_011542120.1:n.*161C>G
XM_005272385.4:c.*161C>G	XP_005272442.1:n.*161C>G
XM_011543817.3:c.*161C>G	XP_011542119.1:n.*161C>G
XM_011543818.2:c.*161C>G	XP_011542120.1:n.*161C>G
XM_017013312.2:c.*161C>G	XP_016868801.1:n.*161C>G
NM_001308093.3:c.*161C>G MANE Select	NP_001295022.1:n.*161C>G
NM_001308094.2:c.*161C>G	NP_001295023.1:n.*161C>G
NM_001374273.1:c.*161C>G	NP_001361202.1:n.*161C>G
NM_001374274.1:c.*161C>G	NP_001361203.1:n.*161C>G
NM_002052.5:c.*161C>G	NP_002043.2:n.*161C>G