Canonical Allele Identifier: CA1400713738

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481050T= , CM000665.2:g.128481050T=	GRCh38
NC_000003.11:g.128199893T= , CM000665.1:g.128199893T=	GRCh37
NC_000003.10:g.129682583T=	NCBI36
NG_029334.1:g.17138A= , LRG_295:g.17138A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1412A= MANE Plus Clinical	ENSP00000417074.1:p.His471=
ENST00000696466.1:c.1694A=	ENSP00000512647.1:p.His565=
ENST00000696672.1:c.387A=	ENSP00000512796.1:p.Pro129=
ENST00000341105.7:c.1412A= MANE Select	ENSP00000345681.2:p.His471=
ENST00000341105.6:c.1412A=	ENSP00000345681.2:p.His471=
ENST00000430265.6:c.1370A=	ENSP00000400259.2:p.His457=
ENST00000487848.5:c.1412A=	ENSP00000417074.1:p.His471=
ENST00000489987.1:n.529A=
NM_001145661.1:c.1412A= , LRG_295t1:c.1412A=	NP_001139133.1:p.His471=
NM_001145662.1:c.1370A=	NP_001139134.1:p.His457=
NM_032638.4:c.1412A= , LRG_295t2:c.1412A=	NP_116027.2:p.His471=
NM_001145661.2:c.1412A= MANE Plus Clinical	NP_001139133.1:p.His471=
NM_032638.5:c.1412A= MANE Select	NP_116027.2:p.His471=