Canonical Allele Identifier: CA1400715238

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481908A= , CM000665.2:g.128481908A=	GRCh38
NC_000003.11:g.128200751A= , CM000665.1:g.128200751A=	GRCh37
NC_000003.10:g.129683441A=	NCBI36
NG_029334.1:g.16280T= , LRG_295:g.16280T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1054T= MANE Plus Clinical	ENSP00000417074.1:p.Cys352=
ENST00000696466.1:c.1336T=	ENSP00000512647.1:p.Cys446=
ENST00000696672.1:c.37T=	ENSP00000512796.1:p.Cys13=
ENST00000341105.7:c.1054T= MANE Select	ENSP00000345681.2:p.Cys352=
ENST00000341105.6:c.1054T=	ENSP00000345681.2:p.Cys352=
ENST00000430265.6:c.1018-6T=	ENSP00000400259.2:n.1018-6T=
ENST00000487848.5:c.1054T=	ENSP00000417074.1:p.Cys352=
ENST00000489987.1:n.171T=
NM_001145661.1:c.1054T= , LRG_295t1:c.1054T=	NP_001139133.1:p.Cys352=
NM_001145662.1:c.1018-6T=	NP_001139134.1:n.1018-6T=
NM_032638.4:c.1054T= , LRG_295t2:c.1054T=	NP_116027.2:p.Cys352=
NM_001145661.2:c.1054T= MANE Plus Clinical	NP_001139133.1:p.Cys352=
NM_032638.5:c.1054T= MANE Select	NP_116027.2:p.Cys352=