Canonical Allele Identifier: CA2758339236

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128484205_128484206insG , CM000665.2:g.128484205_128484206insG	GRCh38
NC_000003.11:g.128203048_128203049insG , CM000665.1:g.128203048_128203049insG	GRCh37
NC_000003.10:g.129685738_129685739insG	NCBI36
NG_029334.1:g.13982_13983insC , LRG_295:g.13982_13983insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.872-201_872-200insC MANE Plus Clinical	ENSP00000417074.1:n.872-201_872-200insC
ENST00000696466.1:c.1154-201_1154-200insC	ENSP00000512647.1:n.1154-201_1154-200insC
ENST00000341105.7:c.872-201_872-200insC MANE Select	ENSP00000345681.2:n.872-201_872-200insC
ENST00000341105.6:c.872-201_872-200insC	ENSP00000345681.2:n.872-201_872-200insC
ENST00000430265.6:c.872-201_872-200insC	ENSP00000400259.2:n.872-201_872-200insC
ENST00000487848.5:c.872-201_872-200insC	ENSP00000417074.1:n.872-201_872-200insC
NM_001145661.1:c.872-201_872-200insC , LRG_295t1:c.872-201_872-200insC	NP_001139133.1:n.872-201_872-200insC
NM_001145662.1:c.872-201_872-200insC	NP_001139134.1:n.872-201_872-200insC
NM_032638.4:c.872-201_872-200insC , LRG_295t2:c.872-201_872-200insC	NP_116027.2:n.872-201_872-200insC
NM_001145661.2:c.872-201_872-200insC MANE Plus Clinical	NP_001139133.1:n.872-201_872-200insC
NM_032638.5:c.872-201_872-200insC MANE Select	NP_116027.2:n.872-201_872-200insC