Canonical Allele Identifier: CA2667540839

Gene: GATA2

Linked Data

• gnomAD v4: 3-128484056-CGGGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128484062_128484065del , CM000665.2:g.128484062_128484065del	GRCh38
NC_000003.11:g.128202905_128202908del , CM000665.1:g.128202905_128202908del	GRCh37
NC_000003.10:g.129685595_129685598del	NCBI36
NG_029334.1:g.14128_14131del , LRG_295:g.14128_14131del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.872-55_872-52del MANE Plus Clinical	ENSP00000417074.1:n.872-55_872-52del
ENST00000696466.1:c.1154-55_1154-52del	ENSP00000512647.1:n.1154-55_1154-52del
ENST00000341105.7:c.872-55_872-52del MANE Select	ENSP00000345681.2:n.872-55_872-52del
ENST00000341105.6:c.872-55_872-52del	ENSP00000345681.2:n.872-55_872-52del
ENST00000430265.6:c.872-55_872-52del	ENSP00000400259.2:n.872-55_872-52del
ENST00000487848.5:c.872-55_872-52del	ENSP00000417074.1:n.872-55_872-52del
NM_001145661.1:c.872-55_872-52del , LRG_295t1:c.872-55_872-52del	NP_001139133.1:n.872-55_872-52del
NM_001145662.1:c.872-55_872-52del	NP_001139134.1:n.872-55_872-52del
NM_032638.4:c.872-55_872-52del , LRG_295t2:c.872-55_872-52del	NP_116027.2:n.872-55_872-52del
NM_001145661.2:c.872-55_872-52del MANE Plus Clinical	NP_001139133.1:n.872-55_872-52del
NM_032638.5:c.872-55_872-52del MANE Select	NP_116027.2:n.872-55_872-52del