Canonical Allele Identifier: CA1400719311
Gene: GATA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128485969_128486044delinsCCGTCCTTGTCCTCTCCTCGGGCTGCACTACCCCCCGCGGAAGATGAGGCTGGAGACGCAGCCCCCGTGGTGCTAG , CM000665.2:g.128485969_128486044delinsCCGTCCTTGTCCTCTCCTCGGGCTGCACTACCCCCCGCGGAAGATGAGGCTGGAGACGCAGCCCCCGTGGTGCTAG GRCh38
NC_000003.11:g.128204812_128204887delinsCCGTCCTTGTCCTCTCCTCGGGCTGCACTACCCCCCGCGGAAGATGAGGCTGGAGACGCAGCCCCCGTGGTGCTAG , CM000665.1:g.128204812_128204887delinsCCGTCCTTGTCCTCTCCTCGGGCTGCACTACCCCCCGCGGAAGATGAGGCTGGAGACGCAGCCCCCGTGGTGCTAG GRCh37
NC_000003.10:g.129687502_129687577delinsCCGTCCTTGTCCTCTCCTCGGGCTGCACTACCCCCCGCGGAAGATGAGGCTGGAGACGCAGCCCCCGTGGTGCTAG NCBI36
NG_029334.1:g.12144_12219delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG , LRG_295:g.12144_12219delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG MANE Plus Clinical ENSP00000417074.1:p.Pro185=
ENST00000696466.1:c.836_911delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG ENSP00000512647.1:p.Pro279=
ENST00000341105.7:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG MANE Select ENSP00000345681.2:p.Pro185=
ENST00000341105.6:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG ENSP00000345681.2:p.Pro185=
ENST00000430265.6:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG ENSP00000400259.2:p.Pro185=
ENST00000487848.5:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG ENSP00000417074.1:p.Pro185=
NM_001145661.1:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG , LRG_295t1:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG NP_001139133.1:p.Pro185=
NM_001145662.1:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG NP_001139134.1:p.Pro185=
NM_032638.4:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG , LRG_295t2:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG NP_116027.2:p.Pro185=
NM_001145661.2:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG MANE Plus Clinical NP_001139133.1:p.Pro185=
NM_032638.5:c.554_629delinsCTAGCACCACGGGGGCTGCGTCTCCAGCCTCATCTTCCGCGGGGGGTAGTGCAGCCCGAGGAGAGGACAAGGACGG MANE Select NP_116027.2:p.Pro185=