Canonical Allele Identifier: CA2838140786
Gene: GATA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128484025_128484026dup , CM000665.2:g.128484025_128484026dup GRCh38
NC_000003.11:g.128202868_128202869dup , CM000665.1:g.128202868_128202869dup GRCh37
NC_000003.10:g.129685558_129685559dup NCBI36
NG_029334.1:g.14166_14167dup , LRG_295:g.14166_14167dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.872-17_872-16dup MANE Plus Clinical ENSP00000417074.1:n.872-17_872-16dup
ENST00000696466.1:c.1154-17_1154-16dup ENSP00000512647.1:n.1154-17_1154-16dup
ENST00000341105.7:c.872-17_872-16dup MANE Select ENSP00000345681.2:n.872-17_872-16dup
ENST00000341105.6:c.872-17_872-16dup ENSP00000345681.2:n.872-17_872-16dup
ENST00000430265.6:c.872-17_872-16dup ENSP00000400259.2:n.872-17_872-16dup
ENST00000487848.5:c.872-17_872-16dup ENSP00000417074.1:n.872-17_872-16dup
NM_001145661.1:c.872-17_872-16dup , LRG_295t1:c.872-17_872-16dup NP_001139133.1:n.872-17_872-16dup
NM_001145662.1:c.872-17_872-16dup NP_001139134.1:n.872-17_872-16dup
NM_032638.4:c.872-17_872-16dup , LRG_295t2:c.872-17_872-16dup NP_116027.2:n.872-17_872-16dup
NM_001145661.2:c.872-17_872-16dup MANE Plus Clinical NP_001139133.1:n.872-17_872-16dup
NM_032638.5:c.872-17_872-16dup MANE Select NP_116027.2:n.872-17_872-16dup