Canonical Allele Identifier: CA2667540537

Gene: GATA2

Linked Data

• gnomAD v4: 3-128481994-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128482000dup , CM000665.2:g.128482000dup	GRCh38
NC_000003.11:g.128200843dup , CM000665.1:g.128200843dup	GRCh37
NC_000003.10:g.129683533dup	NCBI36
NG_029334.1:g.16193dup , LRG_295:g.16193dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1018-51dup MANE Plus Clinical	ENSP00000417074.1:n.1018-51dup
ENST00000696466.1:c.1300-51dup	ENSP00000512647.1:n.1300-51dup
ENST00000341105.7:c.1018-51dup MANE Select	ENSP00000345681.2:n.1018-51dup
ENST00000341105.6:c.1018-51dup	ENSP00000345681.2:n.1018-51dup
ENST00000430265.6:c.1018-93dup	ENSP00000400259.2:n.1018-93dup
ENST00000487848.5:c.1018-51dup	ENSP00000417074.1:n.1018-51dup
ENST00000489987.1:n.84dup
NM_001145661.1:c.1018-51dup , LRG_295t1:c.1018-51dup	NP_001139133.1:n.1018-51dup
NM_001145662.1:c.1018-93dup	NP_001139134.1:n.1018-93dup
NM_032638.4:c.1018-51dup , LRG_295t2:c.1018-51dup	NP_116027.2:n.1018-51dup
NM_001145661.2:c.1018-51dup MANE Plus Clinical	NP_001139133.1:n.1018-51dup
NM_032638.5:c.1018-51dup MANE Select	NP_116027.2:n.1018-51dup