Canonical Allele Identifier: CA2667540381

Gene: GATA2

Linked Data

• gnomAD v4: 3-128481670-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481672del , CM000665.2:g.128481672del	GRCh38
NC_000003.11:g.128200515del , CM000665.1:g.128200515del	GRCh37
NC_000003.10:g.129683205del	NCBI36
NG_029334.1:g.16517del , LRG_295:g.16517del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1143+148del MANE Plus Clinical	ENSP00000417074.1:n.1143+148del
ENST00000696466.1:c.1425+148del	ENSP00000512647.1:n.1425+148del
ENST00000696672.1:c.126+148del	ENSP00000512796.1:n.126+148del
ENST00000341105.7:c.1143+148del MANE Select	ENSP00000345681.2:n.1143+148del
ENST00000341105.6:c.1143+148del	ENSP00000345681.2:n.1143+148del
ENST00000430265.6:c.1101+148del	ENSP00000400259.2:n.1101+148del
ENST00000487848.5:c.1143+148del	ENSP00000417074.1:n.1143+148del
ENST00000489987.1:n.260+148del
NM_001145661.1:c.1143+148del , LRG_295t1:c.1143+148del	NP_001139133.1:n.1143+148del
NM_001145662.1:c.1101+148del	NP_001139134.1:n.1101+148del
NM_032638.4:c.1143+148del , LRG_295t2:c.1143+148del	NP_116027.2:n.1143+148del
NM_001145661.2:c.1143+148del MANE Plus Clinical	NP_001139133.1:n.1143+148del
NM_032638.5:c.1143+148del MANE Select	NP_116027.2:n.1143+148del