Canonical Allele Identifier: CA2667540087
Gene: GATA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128480846_128480892del , CM000665.2:g.128480846_128480892del GRCh38
NC_000003.11:g.128199689_128199735del , CM000665.1:g.128199689_128199735del GRCh37
NC_000003.10:g.129682379_129682425del NCBI36
NG_029334.1:g.17297_17343del , LRG_295:g.17297_17343del

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.*128_*174del MANE Plus Clinical ENSP00000417074.1:n.*128_*174del
ENST00000696466.1:c.*128_*174del ENSP00000512647.1:n.*128_*174del
ENST00000696672.1:c.546_592del ENSP00000512796.1:n.[c.546_592del;Gly183Ter]
ENST00000341105.7:c.*128_*174del MANE Select ENSP00000345681.2:n.*128_*174del
ENST00000341105.6:c.*128_*174del ENSP00000345681.2:n.*128_*174del
ENST00000430265.6:c.*128_*174del ENSP00000400259.2:n.*128_*174del
ENST00000489987.1:n.688_734del
NM_001145661.1:c.*128_*174del , LRG_295t1:c.*128_*174del NP_001139133.1:n.*128_*174del
NM_001145662.1:c.*128_*174del NP_001139134.1:n.*128_*174del
NM_032638.4:c.*128_*174del , LRG_295t2:c.*128_*174del NP_116027.2:n.*128_*174del
NM_001145661.2:c.*128_*174del MANE Plus Clinical NP_001139133.1:n.*128_*174del
NM_032638.5:c.*128_*174del MANE Select NP_116027.2:n.*128_*174del