Canonical Allele Identifier: CA1400713292

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128480669A= , CM000665.2:g.128480669A=	GRCh38
NC_000003.11:g.128199512A= , CM000665.1:g.128199512A=	GRCh37
NC_000003.10:g.129682202A=	NCBI36
NG_029334.1:g.17519T= , LRG_295:g.17519T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.*350T= MANE Plus Clinical	ENSP00000417074.1:n.*350T=
ENST00000696466.1:c.*350T=	ENSP00000512647.1:n.*350T=
ENST00000696672.1:c.768T=	ENSP00000512796.1:n.768T=
ENST00000341105.7:c.*350T= MANE Select	ENSP00000345681.2:n.*350T=
ENST00000341105.6:c.*350T=	ENSP00000345681.2:n.*350T=
ENST00000430265.6:c.*350T=	ENSP00000400259.2:n.*350T=
ENST00000489987.1:n.910T=
NM_001145661.1:c.*350T= , LRG_295t1:c.*350T=	NP_001139133.1:n.*350T=
NM_001145662.1:c.*350T=	NP_001139134.1:n.*350T=
NM_032638.4:c.*350T= , LRG_295t2:c.*350T=	NP_116027.2:n.*350T=
NM_001145661.2:c.*350T= MANE Plus Clinical	NP_001139133.1:n.*350T=
NM_032638.5:c.*350T= MANE Select	NP_116027.2:n.*350T=