Canonical Allele Identifier: CA2667539876

Gene: GATA2

Linked Data

• gnomAD v4: 3-128480640-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128480641del , CM000665.2:g.128480641del	GRCh38
NC_000003.11:g.128199484del , CM000665.1:g.128199484del	GRCh37
NC_000003.10:g.129682174del	NCBI36
NG_029334.1:g.17547del , LRG_295:g.17547del

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.*378del MANE Plus Clinical	ENSP00000417074.1:n.*378del
ENST00000696466.1:c.*378del	ENSP00000512647.1:n.*378del
ENST00000696672.1:c.796del	ENSP00000512796.1:n.796del
ENST00000341105.7:c.*378del MANE Select	ENSP00000345681.2:n.*378del
ENST00000341105.6:c.*378del	ENSP00000345681.2:n.*378del
ENST00000430265.6:c.*378del	ENSP00000400259.2:n.*378del
ENST00000489987.1:n.938del
NM_001145661.1:c.*378del , LRG_295t1:c.*378del	NP_001139133.1:n.*378del
NM_001145662.1:c.*378del	NP_001139134.1:n.*378del
NM_032638.4:c.*378del , LRG_295t2:c.*378del	NP_116027.2:n.*378del
NM_001145661.2:c.*378del MANE Plus Clinical	NP_001139133.1:n.*378del
NM_032638.5:c.*378del MANE Select	NP_116027.2:n.*378del