Canonical Allele Identifier: CA354413657

Gene: GATA2

Linked Data

• MyVariant Identifiers: chr3:g.128200760A>T (hg19) ; chr3:g.128481917A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481917A>T , CM000665.2:g.128481917A>T	GRCh38
NC_000003.11:g.128200760A>T , CM000665.1:g.128200760A>T	GRCh37
NC_000003.10:g.129683450A>T	NCBI36
NG_029334.1:g.16271T>A , LRG_295:g.16271T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1045T>A MANE Plus Clinical	ENSP00000417074.1:p.Cys349Ser
ENST00000696466.1:c.1327T>A	ENSP00000512647.1:p.Cys443Ser
ENST00000696672.1:c.28T>A	ENSP00000512796.1:p.Cys10Ser
ENST00000341105.7:c.1045T>A MANE Select	ENSP00000345681.2:p.Cys349Ser
ENST00000341105.6:c.1045T>A	ENSP00000345681.2:p.Cys349Ser
ENST00000430265.6:c.1018-15T>A	ENSP00000400259.2:n.1018-15T>A
ENST00000487848.5:c.1045T>A	ENSP00000417074.1:p.Cys349Ser
ENST00000489987.1:n.162T>A
NM_001145661.1:c.1045T>A , LRG_295t1:c.1045T>A	NP_001139133.1:p.Cys349Ser
NM_001145662.1:c.1018-15T>A	NP_001139134.1:n.1018-15T>A
NM_032638.4:c.1045T>A , LRG_295t2:c.1045T>A	NP_116027.2:p.Cys349Ser
NM_001145661.2:c.1045T>A MANE Plus Clinical	NP_001139133.1:p.Cys349Ser
NM_032638.5:c.1045T>A MANE Select	NP_116027.2:p.Cys349Ser