Canonical Allele Identifier: CA891841818

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481877delinsGGGT , CM000665.2:g.128481877delinsGGGT	GRCh38
NC_000003.11:g.128200720delinsGGGT , CM000665.1:g.128200720delinsGGGT	GRCh37
NC_000003.10:g.129683410delinsGGGT	NCBI36
NG_029334.1:g.16311delinsACCC , LRG_295:g.16311delinsACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1085delinsACCC MANE Plus Clinical	ENSP00000417074.1:p.Arg362delinsHisPro
ENST00000696466.1:c.1367delinsACCC	ENSP00000512647.1:p.Arg456delinsHisPro
ENST00000696672.1:c.68delinsACCC	ENSP00000512796.1:p.Arg23delinsHisPro
ENST00000341105.7:c.1085delinsACCC MANE Select	ENSP00000345681.2:p.Arg362delinsHisPro
ENST00000341105.6:c.1085delinsACCC	ENSP00000345681.2:p.Arg362delinsHisPro
ENST00000430265.6:c.1043delinsACCC	ENSP00000400259.2:p.Arg348delinsHisPro
ENST00000487848.5:c.1085delinsACCC	ENSP00000417074.1:p.Arg362delinsHisPro
ENST00000489987.1:n.202delinsACCC
NM_001145661.1:c.1085delinsACCC , LRG_295t1:c.1085delinsACCC	NP_001139133.1:p.Arg362delinsHisPro
NM_001145662.1:c.1043delinsACCC	NP_001139134.1:p.Arg348delinsHisPro
NM_032638.4:c.1085delinsACCC , LRG_295t2:c.1085delinsACCC	NP_116027.2:p.Arg362delinsHisPro
NM_001145661.2:c.1085delinsACCC MANE Plus Clinical	NP_001139133.1:p.Arg362delinsHisPro
NM_032638.5:c.1085delinsACCC MANE Select	NP_116027.2:p.Arg362delinsHisPro