Canonical Allele Identifier: CA2667540450

Gene: GATA2

Linked Data

• gnomAD v4: 3-128481725-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481725A>T , CM000665.2:g.128481725A>T	GRCh38
NC_000003.11:g.128200568A>T , CM000665.1:g.128200568A>T	GRCh37
NC_000003.10:g.129683258A>T	NCBI36
NG_029334.1:g.16463T>A , LRG_295:g.16463T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1143+94T>A MANE Plus Clinical	ENSP00000417074.1:n.1143+94T>A
ENST00000696466.1:c.1425+94T>A	ENSP00000512647.1:n.1425+94T>A
ENST00000696672.1:c.126+94T>A	ENSP00000512796.1:n.126+94T>A
ENST00000341105.7:c.1143+94T>A MANE Select	ENSP00000345681.2:n.1143+94T>A
ENST00000341105.6:c.1143+94T>A	ENSP00000345681.2:n.1143+94T>A
ENST00000430265.6:c.1101+94T>A	ENSP00000400259.2:n.1101+94T>A
ENST00000487848.5:c.1143+94T>A	ENSP00000417074.1:n.1143+94T>A
ENST00000489987.1:n.260+94T>A
NM_001145661.1:c.1143+94T>A , LRG_295t1:c.1143+94T>A	NP_001139133.1:n.1143+94T>A
NM_001145662.1:c.1101+94T>A	NP_001139134.1:n.1101+94T>A
NM_032638.4:c.1143+94T>A , LRG_295t2:c.1143+94T>A	NP_116027.2:n.1143+94T>A
NM_001145661.2:c.1143+94T>A MANE Plus Clinical	NP_001139133.1:n.1143+94T>A
NM_032638.5:c.1143+94T>A MANE Select	NP_116027.2:n.1143+94T>A