Canonical Allele Identifier: CA2502466036
Gene: GATA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128482191_128482192insATTCTCCTCTGTAGCTCTTGCAATCCCGTTGATTAGAACTCTCAGAAGCCTGATGTTAGAATCAACGGGATTGCAAGAGCTA , CM000665.2:g.128482191_128482192insATTCTCCTCTGTAGCTCTTGCAATCCCGTTGATTAGAACTCTCAGAAGCCTGATGTTAGAATCAACGGGATTGCAAGAGCTA GRCh38
NC_000003.11:g.128201034_128201035insATTCTCCTCTGTAGCTCTTGCAATCCCGTTGATTAGAACTCTCAGAAGCCTGATGTTAGAATCAACGGGATTGCAAGAGCTA , CM000665.1:g.128201034_128201035insATTCTCCTCTGTAGCTCTTGCAATCCCGTTGATTAGAACTCTCAGAAGCCTGATGTTAGAATCAACGGGATTGCAAGAGCTA GRCh37
NC_000003.10:g.129683724_129683725insATTCTCCTCTGTAGCTCTTGCAATCCCGTTGATTAGAACTCTCAGAAGCCTGATGTTAGAATCAACGGGATTGCAAGAGCTA NCBI36
NG_029334.1:g.16044_16045insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT , LRG_295:g.16044_16045insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT

Transcript Alleles

HGVS Amino-acid change
ENST00000487848.6:c.1018-200_1018-199insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT MANE Plus Clinical ENSP00000417074.1:n.1018-200_1018-199insA...
ENST00000696466.1:c.1300-200_1300-199insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT ENSP00000512647.1:n.1300-200_1300-199insA...
ENST00000341105.7:c.1018-200_1018-199insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT MANE Select ENSP00000345681.2:n.1018-200_1018-199insA...
ENST00000341105.6:c.1018-200_1018-199insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT ENSP00000345681.2:n.1018-200_1018-199insA...
ENST00000430265.6:c.1018-242_1018-241insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT ENSP00000400259.2:n.1018-242_1018-241insA...
ENST00000487848.5:c.1018-200_1018-199insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT ENSP00000417074.1:n.1018-200_1018-199insA...
NM_001145661.1:c.1018-200_1018-199insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT , LRG_295t1:c.1018-200_1018-199insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT NP_001139133.1:n.1018-200_1018-199insAATC...
NM_001145662.1:c.1018-242_1018-241insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT NP_001139134.1:n.1018-242_1018-241insAATC...
NM_032638.4:c.1018-200_1018-199insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT , LRG_295t2:c.1018-200_1018-199insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT NP_116027.2:n.1018-200_1018-199insAATCAAC...
NM_001145661.2:c.1018-200_1018-199insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT MANE Plus Clinical NP_001139133.1:n.1018-200_1018-199insAATC...
NM_032638.5:c.1018-200_1018-199insAATCAACGGGATTGCAAGAGCTACAGAGGAGAATTAGCTCTTGCAATCCCGTTGATTCTAACATCAGGCTTCTGAGAGTTCT MANE Select NP_116027.2:n.1018-200_1018-199insAATCAAC...