Canonical Allele Identifier: CA1400713662

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481022G= , CM000665.2:g.128481022G=	GRCh38
NC_000003.11:g.128199865G= , CM000665.1:g.128199865G=	GRCh37
NC_000003.10:g.129682555G=	NCBI36
NG_029334.1:g.17166C= , LRG_295:g.17166C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1440C= MANE Plus Clinical	ENSP00000417074.1:p.Gly480=
ENST00000696466.1:c.1722C=	ENSP00000512647.1:p.Gly574=
ENST00000696672.1:c.415C=	ENSP00000512796.1:p.Leu139=
ENST00000341105.7:c.1440C= MANE Select	ENSP00000345681.2:p.Gly480=
ENST00000341105.6:c.1440C=	ENSP00000345681.2:p.Gly480=
ENST00000430265.6:c.1398C=	ENSP00000400259.2:p.Gly466=
ENST00000487848.5:c.1440C=	ENSP00000417074.1:p.Gly480=
ENST00000489987.1:n.557C=
NM_001145661.1:c.1440C= , LRG_295t1:c.1440C=	NP_001139133.1:p.Gly480=
NM_001145662.1:c.1398C=	NP_001139134.1:p.Gly466=
NM_032638.4:c.1440C= , LRG_295t2:c.1440C=	NP_116027.2:p.Gly480=
NM_001145661.2:c.1440C= MANE Plus Clinical	NP_001139133.1:p.Gly480=
NM_032638.5:c.1440C= MANE Select	NP_116027.2:p.Gly480=