Canonical Allele Identifier: CA1400715598
Gene: GATA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128482084_128482085delinsAC , CM000665.2:g.128482084_128482085delinsAC GRCh38
NC_000003.11:g.128200927_128200928delinsAC , CM000665.1:g.128200927_128200928delinsAC GRCh37
NC_000003.10:g.129683617_129683618delinsAC NCBI36
NG_029334.1:g.16103_16104delinsGT , LRG_295:g.16103_16104delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000487848.6:c.1018-141_1018-140delinsGT MANE Plus Clinical ENSP00000417074.1:n.1018-141_1018-140deli...
ENST00000696466.1:c.1300-141_1300-140delinsGT ENSP00000512647.1:n.1300-141_1300-140deli...
ENST00000341105.7:c.1018-141_1018-140delinsGT MANE Select ENSP00000345681.2:n.1018-141_1018-140deli...
ENST00000341105.6:c.1018-141_1018-140delinsGT ENSP00000345681.2:n.1018-141_1018-140deli...
ENST00000430265.6:c.1018-183_1018-182delinsGT ENSP00000400259.2:n.1018-183_1018-182deli...
ENST00000487848.5:c.1018-141_1018-140delinsGT ENSP00000417074.1:n.1018-141_1018-140deli...
NM_001145661.1:c.1018-141_1018-140delinsGT , LRG_295t1:c.1018-141_1018-140delinsGT NP_001139133.1:n.1018-141_1018-140delinsG...
NM_001145662.1:c.1018-183_1018-182delinsGT NP_001139134.1:n.1018-183_1018-182delinsG...
NM_032638.4:c.1018-141_1018-140delinsGT , LRG_295t2:c.1018-141_1018-140delinsGT NP_116027.2:n.1018-141_1018-140delinsGT
NM_001145661.2:c.1018-141_1018-140delinsGT MANE Plus Clinical NP_001139133.1:n.1018-141_1018-140delinsG...
NM_032638.5:c.1018-141_1018-140delinsGT MANE Select NP_116027.2:n.1018-141_1018-140delinsGT