Canonical Allele Identifier: CA2667539469

Gene: GATA2

Linked Data

• gnomAD v4: 3-128480332-A-ATCT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128480332_128480333insTCT , CM000665.2:g.128480332_128480333insTCT	GRCh38
NC_000003.11:g.128199175_128199176insTCT , CM000665.1:g.128199175_128199176insTCT	GRCh37
NC_000003.10:g.129681865_129681866insTCT	NCBI36
NG_029334.1:g.17855_17856insAGA , LRG_295:g.17855_17856insAGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.*686_*687insAGA MANE Plus Clinical	ENSP00000417074.1:n.*686_*687insAGA
ENST00000696466.1:c.*686_*687insAGA	ENSP00000512647.1:n.*686_*687insAGA
ENST00000696672.1:c.1104_1105insAGA	ENSP00000512796.1:n.1104_1105insAGA
ENST00000341105.7:c.*686_*687insAGA MANE Select	ENSP00000345681.2:n.*686_*687insAGA
ENST00000341105.6:c.*686_*687insAGA	ENSP00000345681.2:n.*686_*687insAGA
ENST00000430265.6:c.*686_*687insAGA	ENSP00000400259.2:n.*686_*687insAGA
ENST00000489987.1:n.1246_1247insAGA
NM_001145661.1:c.*686_*687insAGA , LRG_295t1:c.*686_*687insAGA	NP_001139133.1:n.*686_*687insAGA
NM_001145662.1:c.*686_*687insAGA	NP_001139134.1:n.*686_*687insAGA
NM_032638.4:c.*686_*687insAGA , LRG_295t2:c.*686_*687insAGA	NP_116027.2:n.*686_*687insAGA
NM_001145661.2:c.*686_*687insAGA MANE Plus Clinical	NP_001139133.1:n.*686_*687insAGA
NM_032638.5:c.*686_*687insAGA MANE Select	NP_116027.2:n.*686_*687insAGA