Canonical Allele Identifier: CA2686162412

Gene: GATA4

Linked Data

• gnomAD v4: 8-11708261-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11708261C>A , CM000670.2:g.11708261C>A	GRCh38
NC_000008.10:g.11565770C>A , CM000670.1:g.11565770C>A	GRCh37
NC_000008.9:g.11603179C>A	NCBI36
NG_008177.2:g.36343C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.-52C>A	ENSP00000482268.2:n.-52C>A
ENST00000532059.6:c.-52C>A MANE Select	ENSP00000435712.1:n.-52C>A
ENST00000335135.8:c.-52C>A	ENSP00000334458.4:n.-52C>A
ENST00000526716.5:c.-6+3957C>A	ENSP00000435347.1:n.-6+3957C>A
ENST00000526974.1:c.-52C>A	ENSP00000473598.1:n.-52C>A
ENST00000528027.1:c.-52C>A	ENSP00000432278.1:n.-52C>A
ENST00000528712.5:c.-6+7483C>A	ENSP00000435043.1:n.-6+7483C>A
ENST00000532059.5:c.-52C>A	ENSP00000435712.1:n.-52C>A
ENST00000532977.1:c.-52C>A	ENSP00000473671.1:n.-52C>A
NM_001308093.1:c.-52C>A	NP_001295022.1:n.-52C>A
NM_001308094.1:c.-6+7483C>A	NP_001295023.1:n.-6+7483C>A
NM_002052.3:c.-52C>A	NP_002043.2:n.-52C>A
NM_002052.4:c.-52C>A	NP_002043.2:n.-52C>A
XM_005272385.3:c.-52C>A	XP_005272442.1:n.-52C>A
XM_005272386.1:c.-52C>A	XP_005272443.1:n.-52C>A
XM_006716248.1:c.-52C>A	XP_006716311.1:n.-52C>A
XM_011543817.1:c.-52C>A	XP_011542119.1:n.-52C>A
XM_011543818.1:c.-52C>A	XP_011542120.1:n.-52C>A
XM_005272385.4:c.-52C>A	XP_005272442.1:n.-52C>A
XM_011543817.3:c.-52C>A	XP_011542119.1:n.-52C>A
XM_011543818.2:c.-52C>A	XP_011542120.1:n.-52C>A
XM_017013312.2:c.-52C>A	XP_016868801.1:n.-52C>A
NM_001308093.3:c.-52C>A MANE Select	NP_001295022.1:n.-52C>A
NM_001308094.2:c.-6+7483C>A	NP_001295023.1:n.-6+7483C>A
NM_001374273.1:c.-3+3957C>A	NP_001361202.1:n.-3+3957C>A
NM_001374274.1:c.-3+247C>A	NP_001361203.1:n.-3+247C>A
NM_002052.5:c.-52C>A	NP_002043.2:n.-52C>A