Canonical Allele Identifier: CA1400713351

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128480735_128480736delinsTC , CM000665.2:g.128480735_128480736delinsTC	GRCh38
NC_000003.11:g.128199578_128199579delinsTC , CM000665.1:g.128199578_128199579delinsTC	GRCh37
NC_000003.10:g.129682268_129682269delinsTC	NCBI36
NG_029334.1:g.17452_17453delinsGA , LRG_295:g.17452_17453delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.*283_*284delinsGA MANE Plus Clinical	ENSP00000417074.1:n.*283_*284delinsGA
ENST00000696466.1:c.*283_*284delinsGA	ENSP00000512647.1:n.*283_*284delinsGA
ENST00000696672.1:c.701_702delinsGA	ENSP00000512796.1:n.701_702delinsGA
ENST00000341105.7:c.*283_*284delinsGA MANE Select	ENSP00000345681.2:n.*283_*284delinsGA
ENST00000341105.6:c.*283_*284delinsGA	ENSP00000345681.2:n.*283_*284delinsGA
ENST00000430265.6:c.*283_*284delinsGA	ENSP00000400259.2:n.*283_*284delinsGA
ENST00000489987.1:n.843_844delinsGA
NM_001145661.1:c.*283_*284delinsGA , LRG_295t1:c.*283_*284delinsGA	NP_001139133.1:n.*283_*284delinsGA
NM_001145662.1:c.*283_*284delinsGA	NP_001139134.1:n.*283_*284delinsGA
NM_032638.4:c.*283_*284delinsGA , LRG_295t2:c.*283_*284delinsGA	NP_116027.2:n.*283_*284delinsGA
NM_001145661.2:c.*283_*284delinsGA MANE Plus Clinical	NP_001139133.1:n.*283_*284delinsGA
NM_032638.5:c.*283_*284delinsGA MANE Select	NP_116027.2:n.*283_*284delinsGA