Canonical Allele Identifier: CA2686162488

Gene: GATA4

Linked Data

• gnomAD v4: 8-11708429-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11708432del , CM000670.2:g.11708432del	GRCh38
NC_000008.10:g.11565941del , CM000670.1:g.11565941del	GRCh37
NC_000008.9:g.11603350del	NCBI36
NG_008177.2:g.36514del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622443.3:c.120del	ENSP00000482268.2:p.Thr41HisfsTer?
ENST00000532059.6:c.120del MANE Select	ENSP00000435712.1:p.Thr41HisfsTer?
ENST00000335135.8:c.120del	ENSP00000334458.4:p.Thr41HisfsTer?
ENST00000526716.5:c.-6+4128del	ENSP00000435347.1:n.-6+4128del
ENST00000528027.1:c.120del	ENSP00000432278.1:p.Thr41HisfsTer?
ENST00000528712.5:c.-6+7654del	ENSP00000435043.1:n.-6+7654del
ENST00000532059.5:c.120del	ENSP00000435712.1:p.Thr41HisfsTer?
ENST00000622443.2:c.119del	ENSP00000482268.1:p.Pro40HisfsTer?
NM_001308093.1:c.120del	NP_001295022.1:p.Thr41HisfsTer?
NM_001308094.1:c.-6+7654del	NP_001295023.1:n.-6+7654del
NM_002052.3:c.120del	NP_002043.2:p.Thr41HisfsTer?
NM_002052.4:c.120del	NP_002043.2:p.Thr41HisfsTer?
XM_005272385.3:c.120del	XP_005272442.1:p.Thr41HisfsTer?
XM_005272386.1:c.120del	XP_005272443.1:p.Thr41HisfsTer?
XM_006716248.1:c.120del	XP_006716311.1:p.Thr41HisfsTer?
XM_011543817.1:c.120del	XP_011542119.1:p.Thr41HisfsTer?
XM_011543818.1:c.120del	XP_011542120.1:p.Thr41HisfsTer?
XM_005272385.4:c.120del	XP_005272442.1:p.Thr41HisfsTer?
XM_011543817.3:c.120del	XP_011542119.1:p.Thr41HisfsTer?
XM_011543818.2:c.120del	XP_011542120.1:p.Thr41HisfsTer?
XM_017013312.2:c.120del	XP_016868801.1:p.Thr41HisfsTer?
NM_001308093.3:c.120del MANE Select	NP_001295022.1:p.Thr41HisfsTer?
NM_001308094.2:c.-6+7654del	NP_001295023.1:n.-6+7654del
NM_001374273.1:c.-3+4128del	NP_001361202.1:n.-3+4128del
NM_001374274.1:c.-3+418del	NP_001361203.1:n.-3+418del
NM_002052.5:c.120del	NP_002043.2:p.Thr41HisfsTer?