Canonical Allele Identifier: CA645523653
Gene: GATA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128486359dup , CM000665.2:g.128486359dup GRCh38
NC_000003.11:g.128205202dup , CM000665.1:g.128205202dup GRCh37
NC_000003.10:g.129687892dup NCBI36
NG_029334.1:g.11830dup , LRG_295:g.11830dup

Transcript Alleles

HGVS Amino-acid change
ENST00000487848.6:c.240dup MANE Plus Clinical ENSP00000417074.1:p.Gly81ArgfsTer?
ENST00000696466.1:c.522dup ENSP00000512647.1:p.Gly175ArgfsTer?
ENST00000341105.7:c.240dup MANE Select ENSP00000345681.2:p.Gly81ArgfsTer?
ENST00000341105.6:c.240dup ENSP00000345681.2:p.Gly81ArgfsTer?
ENST00000430265.6:c.240dup ENSP00000400259.2:p.Gly81ArgfsTer?
ENST00000487848.5:c.240dup ENSP00000417074.1:p.Gly81ArgfsTer?
ENST00000492608.1:c.240dup ENSP00000418132.1:p.Gly81ArgfsTer?
NM_001145661.1:c.240dup , LRG_295t1:c.240dup NP_001139133.1:p.Gly81ArgfsTer?
NM_001145662.1:c.240dup NP_001139134.1:p.Gly81ArgfsTer?
NM_032638.4:c.240dup , LRG_295t2:c.240dup NP_116027.2:p.Gly81ArgfsTer?
NM_001145661.2:c.240dup MANE Plus Clinical NP_001139133.1:p.Gly81ArgfsTer?
NM_032638.5:c.240dup MANE Select NP_116027.2:p.Gly81ArgfsTer?