Canonical Allele Identifier: CA1400717764

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128484203_128484204delinsCG , CM000665.2:g.128484203_128484204delinsCG	GRCh38
NC_000003.11:g.128203046_128203047delinsCG , CM000665.1:g.128203046_128203047delinsCG	GRCh37
NC_000003.10:g.129685736_129685737delinsCG	NCBI36
NG_029334.1:g.13984_13985delinsCG , LRG_295:g.13984_13985delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.872-199_872-198delinsCG MANE Plus Clinical	ENSP00000417074.1:n.872-199_872-198delinsCG
ENST00000696466.1:c.1154-199_1154-198delinsCG	ENSP00000512647.1:n.1154-199_1154-198delinsCG
ENST00000341105.7:c.872-199_872-198delinsCG MANE Select	ENSP00000345681.2:n.872-199_872-198delinsCG
ENST00000341105.6:c.872-199_872-198delinsCG	ENSP00000345681.2:n.872-199_872-198delinsCG
ENST00000430265.6:c.872-199_872-198delinsCG	ENSP00000400259.2:n.872-199_872-198delinsCG
ENST00000487848.5:c.872-199_872-198delinsCG	ENSP00000417074.1:n.872-199_872-198delinsCG
NM_001145661.1:c.872-199_872-198delinsCG , LRG_295t1:c.872-199_872-198delinsCG	NP_001139133.1:n.872-199_872-198delinsCG
NM_001145662.1:c.872-199_872-198delinsCG	NP_001139134.1:n.872-199_872-198delinsCG
NM_032638.4:c.872-199_872-198delinsCG , LRG_295t2:c.872-199_872-198delinsCG	NP_116027.2:n.872-199_872-198delinsCG
NM_001145661.2:c.872-199_872-198delinsCG MANE Plus Clinical	NP_001139133.1:n.872-199_872-198delinsCG
NM_032638.5:c.872-199_872-198delinsCG MANE Select	NP_116027.2:n.872-199_872-198delinsCG