Canonical Allele Identifier: CA3263392435

Gene: GATA4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11757011_11757012insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT , CM000670.2:g.11757011_11757012insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	GRCh38
NC_000008.10:g.11614520_11614521insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT , CM000670.1:g.11614520_11614521insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	GRCh37
NC_000008.9:g.11651929_11651930insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	NCBI36
NG_008177.2:g.85093_85094insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT

Transcript Alleles

HGVS	Amino-acid Change
NM_001308093.3:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT MANE Select	NP_001295022.1:p.Glu360Ter
ENST00000532059.6:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT MANE Select	ENSP00000435712.1:p.Glu360Ter
NM_001308093.1:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	NP_001295022.1:p.Glu360Ter
NM_001308094.1:c.456_457insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	NP_001295023.1:p.Glu153Ter
NM_001308094.2:c.456_457insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	NP_001295023.1:p.Glu153Ter
NM_001374273.1:c.456_457insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	NP_001361202.1:p.Glu153Ter
NM_001374274.1:c.330_331insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	NP_001361203.1:p.Glu111Ter
NM_002052.3:c.1074_1075insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	NP_002043.2:p.Glu359Ter
NM_002052.4:c.1074_1075insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	NP_002043.2:p.Glu359Ter
NM_002052.5:c.1074_1075insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	NP_002043.2:p.Glu359Ter
ENST00000335135.8:c.1074_1075insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	ENSP00000334458.4:p.Glu359Ter
ENST00000526021.1:n.519_520insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT
ENST00000526716.5:c.456_457insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	ENSP00000435347.1:p.Glu153Ter
ENST00000528712.5:c.456_457insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	ENSP00000435043.1:p.Glu153Ter
ENST00000532059.5:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	ENSP00000435712.1:p.Glu360Ter
ENST00000622443.2:c.1071_1072insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	ENSP00000482268.1:p.Glu358Ter
ENST00000622443.3:c.1074_1075insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	ENSP00000482268.2:p.Glu359Ter
XM_005272385.3:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	XP_005272442.1:p.Glu360Ter
XM_005272385.4:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	XP_005272442.1:p.Glu360Ter
XM_005272386.1:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	XP_005272443.1:p.Glu360Ter
XM_006716248.1:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	XP_006716311.1:p.Glu360Ter
XM_011543817.1:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	XP_011542119.1:p.Glu360Ter
XM_011543817.3:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	XP_011542119.1:p.Glu360Ter
XM_011543818.1:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	XP_011542120.1:p.Glu360Ter
XM_011543818.2:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	XP_011542120.1:p.Glu360Ter
XM_017013312.2:c.1077_1078insTGACCCACGGTCTTCCCCAGCCTCATGATTGCTCTTTTAAGTGAGCCATCCT	XP_016868801.1:p.Glu360Ter