Canonical Allele Identifier: CA1400714210
Gene: GATA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128481240T= , CM000665.2:g.128481240T= GRCh38
NC_000003.11:g.128200083T= , CM000665.1:g.128200083T= GRCh37
NC_000003.10:g.129682773T= NCBI36
NG_029334.1:g.16948A= , LRG_295:g.16948A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.1222A= MANE Plus Clinical ENSP00000417074.1:p.Lys408=
ENST00000696466.1:c.1504A= ENSP00000512647.1:p.Lys502=
ENST00000696672.1:c.197A= ENSP00000512796.1:p.Gln66=
ENST00000341105.7:c.1222A= MANE Select ENSP00000345681.2:p.Lys408=
ENST00000341105.6:c.1222A= ENSP00000345681.2:p.Lys408=
ENST00000430265.6:c.1180A= ENSP00000400259.2:p.Lys394=
ENST00000487848.5:c.1222A= ENSP00000417074.1:p.Lys408=
ENST00000489987.1:n.339A=
NM_001145661.1:c.1222A= , LRG_295t1:c.1222A= NP_001139133.1:p.Lys408=
NM_001145662.1:c.1180A= NP_001139134.1:p.Lys394=
NM_032638.4:c.1222A= , LRG_295t2:c.1222A= NP_116027.2:p.Lys408=
NM_001145661.2:c.1222A= MANE Plus Clinical NP_001139133.1:p.Lys408=
NM_032638.5:c.1222A= MANE Select NP_116027.2:p.Lys408=