Canonical Allele Identifier: CA2667541073
Gene: GATA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128486198_128486206dup , CM000665.2:g.128486198_128486206dup GRCh38
NC_000003.11:g.128205041_128205049dup , CM000665.1:g.128205041_128205049dup GRCh37
NC_000003.10:g.129687731_129687739dup NCBI36
NG_029334.1:g.11992_12000dup , LRG_295:g.11992_12000dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.402_410dup MANE Plus Clinical ENSP00000417074.1:p.Pro137_Leu138insGlyGlyPro
ENST00000696466.1:c.684_692dup ENSP00000512647.1:p.Pro231_Leu232insGlyGlyPro
ENST00000341105.7:c.402_410dup MANE Select ENSP00000345681.2:p.Pro137_Leu138insGlyGlyPro
ENST00000341105.6:c.402_410dup ENSP00000345681.2:p.Pro137_Leu138insGlyGlyPro
ENST00000430265.6:c.402_410dup ENSP00000400259.2:p.Pro137_Leu138insGlyGlyPro
ENST00000487848.5:c.402_410dup ENSP00000417074.1:p.Pro137_Leu138insGlyGlyPro
ENST00000492608.1:c.402_410dup ENSP00000418132.1:p.Pro137_Leu138insGlyGlyPro
NM_001145661.1:c.402_410dup , LRG_295t1:c.402_410dup NP_001139133.1:p.Pro137_Leu138insGlyGlyPro
NM_001145662.1:c.402_410dup NP_001139134.1:p.Pro137_Leu138insGlyGlyPro
NM_032638.4:c.402_410dup , LRG_295t2:c.402_410dup NP_116027.2:p.Pro137_Leu138insGlyGlyPro
NM_001145661.2:c.402_410dup MANE Plus Clinical NP_001139133.1:p.Pro137_Leu138insGlyGlyPro
NM_032638.5:c.402_410dup MANE Select NP_116027.2:p.Pro137_Leu138insGlyGlyPro