Canonical Allele Identifier: CA1400713609

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128480982_128480983delinsTC , CM000665.2:g.128480982_128480983delinsTC	GRCh38
NC_000003.11:g.128199825_128199826delinsTC , CM000665.1:g.128199825_128199826delinsTC	GRCh37
NC_000003.10:g.129682515_129682516delinsTC	NCBI36
NG_029334.1:g.17205_17206delinsGA , LRG_295:g.17205_17206delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.*36_*37delinsGA MANE Plus Clinical	ENSP00000417074.1:n.*36_*37delinsGA
ENST00000696466.1:c.*36_*37delinsGA	ENSP00000512647.1:n.*36_*37delinsGA
ENST00000696672.1:c.454_455delinsGA	ENSP00000512796.1:p.Asp152=
ENST00000341105.7:c.*36_*37delinsGA MANE Select	ENSP00000345681.2:n.*36_*37delinsGA
ENST00000341105.6:c.*36_*37delinsGA	ENSP00000345681.2:n.*36_*37delinsGA
ENST00000430265.6:c.*36_*37delinsGA	ENSP00000400259.2:n.*36_*37delinsGA
ENST00000489987.1:n.596_597delinsGA
NM_001145661.1:c.*36_*37delinsGA , LRG_295t1:c.*36_*37delinsGA	NP_001139133.1:n.*36_*37delinsGA
NM_001145662.1:c.*36_*37delinsGA	NP_001139134.1:n.*36_*37delinsGA
NM_032638.4:c.*36_*37delinsGA , LRG_295t2:c.*36_*37delinsGA	NP_116027.2:n.*36_*37delinsGA
NM_001145661.2:c.*36_*37delinsGA MANE Plus Clinical	NP_001139133.1:n.*36_*37delinsGA
NM_032638.5:c.*36_*37delinsGA MANE Select	NP_116027.2:n.*36_*37delinsGA