Canonical Allele Identifier: CA2667540730

Gene: GATA2

Linked Data

• gnomAD v4: 3-128482211-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128482216dup , CM000665.2:g.128482216dup	GRCh38
NC_000003.11:g.128201059dup , CM000665.1:g.128201059dup	GRCh37
NC_000003.10:g.129683749dup	NCBI36
NG_029334.1:g.15976dup , LRG_295:g.15976dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1018-268dup MANE Plus Clinical	ENSP00000417074.1:n.1018-268dup
ENST00000696466.1:c.1300-268dup	ENSP00000512647.1:n.1300-268dup
ENST00000341105.7:c.1018-268dup MANE Select	ENSP00000345681.2:n.1018-268dup
ENST00000341105.6:c.1018-268dup	ENSP00000345681.2:n.1018-268dup
ENST00000430265.6:c.1018-310dup	ENSP00000400259.2:n.1018-310dup
ENST00000487848.5:c.1018-268dup	ENSP00000417074.1:n.1018-268dup
NM_001145661.1:c.1018-268dup , LRG_295t1:c.1018-268dup	NP_001139133.1:n.1018-268dup
NM_001145662.1:c.1018-310dup	NP_001139134.1:n.1018-310dup
NM_032638.4:c.1018-268dup , LRG_295t2:c.1018-268dup	NP_116027.2:n.1018-268dup
NM_001145661.2:c.1018-268dup MANE Plus Clinical	NP_001139133.1:n.1018-268dup
NM_032638.5:c.1018-268dup MANE Select	NP_116027.2:n.1018-268dup