Canonical Allele Identifier: CA2577890740
Gene: GATA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128484047del , CM000665.2:g.128484047del GRCh38
NC_000003.11:g.128202890del , CM000665.1:g.128202890del GRCh37
NC_000003.10:g.129685580del NCBI36
NG_029334.1:g.14142del , LRG_295:g.14142del

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.872-41del MANE Plus Clinical ENSP00000417074.1:n.872-41del
ENST00000696466.1:c.1154-41del ENSP00000512647.1:n.1154-41del
ENST00000341105.7:c.872-41del MANE Select ENSP00000345681.2:n.872-41del
ENST00000341105.6:c.872-41del ENSP00000345681.2:n.872-41del
ENST00000430265.6:c.872-41del ENSP00000400259.2:n.872-41del
ENST00000487848.5:c.872-41del ENSP00000417074.1:n.872-41del
NM_001145661.1:c.872-41del , LRG_295t1:c.872-41del NP_001139133.1:n.872-41del
NM_001145662.1:c.872-41del NP_001139134.1:n.872-41del
NM_032638.4:c.872-41del , LRG_295t2:c.872-41del NP_116027.2:n.872-41del
NM_001145661.2:c.872-41del MANE Plus Clinical NP_001139133.1:n.872-41del
NM_032638.5:c.872-41del MANE Select NP_116027.2:n.872-41del