Canonical Allele Identifier: CA1400713340

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128480726C= , CM000665.2:g.128480726C=	GRCh38
NC_000003.11:g.128199569C= , CM000665.1:g.128199569C=	GRCh37
NC_000003.10:g.129682259C=	NCBI36
NG_029334.1:g.17462G= , LRG_295:g.17462G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.*293G= MANE Plus Clinical	ENSP00000417074.1:n.*293G=
ENST00000696466.1:c.*293G=	ENSP00000512647.1:n.*293G=
ENST00000696672.1:c.711G=	ENSP00000512796.1:n.711G=
ENST00000341105.7:c.*293G= MANE Select	ENSP00000345681.2:n.*293G=
ENST00000341105.6:c.*293G=	ENSP00000345681.2:n.*293G=
ENST00000430265.6:c.*293G=	ENSP00000400259.2:n.*293G=
ENST00000489987.1:n.853G=
NM_001145661.1:c.*293G= , LRG_295t1:c.*293G=	NP_001139133.1:n.*293G=
NM_001145662.1:c.*293G=	NP_001139134.1:n.*293G=
NM_032638.4:c.*293G= , LRG_295t2:c.*293G=	NP_116027.2:n.*293G=
NM_001145661.2:c.*293G= MANE Plus Clinical	NP_001139133.1:n.*293G=
NM_032638.5:c.*293G= MANE Select	NP_116027.2:n.*293G=