Canonical Allele Identifier: CA2667539851
Gene: GATA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128480625_128480626insT , CM000665.2:g.128480625_128480626insT GRCh38
NC_000003.11:g.128199468_128199469insT , CM000665.1:g.128199468_128199469insT GRCh37
NC_000003.10:g.129682158_129682159insT NCBI36
NG_029334.1:g.17562_17563insA , LRG_295:g.17562_17563insA

Transcript Alleles

HGVS Amino-acid change
ENST00000487848.6:c.*393_*394insA MANE Plus Clinical ENSP00000417074.1:n.*393_*394insA
ENST00000696466.1:c.*393_*394insA ENSP00000512647.1:n.*393_*394insA
ENST00000696672.1:c.811_812insA ENSP00000512796.1:n.811_812insA
ENST00000341105.7:c.*393_*394insA MANE Select ENSP00000345681.2:n.*393_*394insA
ENST00000341105.6:c.*393_*394insA ENSP00000345681.2:n.*393_*394insA
ENST00000430265.6:c.*393_*394insA ENSP00000400259.2:n.*393_*394insA
ENST00000489987.1:n.953_954insA
NM_001145661.1:c.*393_*394insA , LRG_295t1:c.*393_*394insA NP_001139133.1:n.*393_*394insA
NM_001145662.1:c.*393_*394insA NP_001139134.1:n.*393_*394insA
NM_032638.4:c.*393_*394insA , LRG_295t2:c.*393_*394insA NP_116027.2:n.*393_*394insA
NM_001145661.2:c.*393_*394insA MANE Plus Clinical NP_001139133.1:n.*393_*394insA
NM_032638.5:c.*393_*394insA MANE Select NP_116027.2:n.*393_*394insA