Canonical Allele Identifier: CA1400718472
Gene: GATA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128485229_128485230delinsTC , CM000665.2:g.128485229_128485230delinsTC GRCh38
NC_000003.11:g.128204072_128204073delinsTC , CM000665.1:g.128204072_128204073delinsTC GRCh37
NC_000003.10:g.129686762_129686763delinsTC NCBI36
NG_029334.1:g.12958_12959delinsGA , LRG_295:g.12958_12959delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000487848.6:c.871+497_871+498delinsGA MANE Plus Clinical ENSP00000417074.1:n.871+497_871+498delinsGA
ENST00000696466.1:c.1153+497_1153+498delinsGA ENSP00000512647.1:n.1153+497_1153+498delinsGA
ENST00000341105.7:c.871+497_871+498delinsGA MANE Select ENSP00000345681.2:n.871+497_871+498delinsGA
ENST00000341105.6:c.871+497_871+498delinsGA ENSP00000345681.2:n.871+497_871+498delinsGA
ENST00000430265.6:c.871+497_871+498delinsGA ENSP00000400259.2:n.871+497_871+498delinsGA
ENST00000487848.5:c.871+497_871+498delinsGA ENSP00000417074.1:n.871+497_871+498delinsGA
NM_001145661.1:c.871+497_871+498delinsGA , LRG_295t1:c.871+497_871+498delinsGA NP_001139133.1:n.871+497_871+498delinsGA
NM_001145662.1:c.871+497_871+498delinsGA NP_001139134.1:n.871+497_871+498delinsGA
NM_032638.4:c.871+497_871+498delinsGA , LRG_295t2:c.871+497_871+498delinsGA NP_116027.2:n.871+497_871+498delinsGA
NM_001145661.2:c.871+497_871+498delinsGA MANE Plus Clinical NP_001139133.1:n.871+497_871+498delinsGA
NM_032638.5:c.871+497_871+498delinsGA MANE Select NP_116027.2:n.871+497_871+498delinsGA