Canonical Allele Identifier: CA1400718695

Gene: GATA2

Linked Data

• dbSNP Id: rs2068682784

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128485532_128485534del , CM000665.2:g.128485532_128485534del	GRCh38
NC_000003.11:g.128204375_128204377del , CM000665.1:g.128204375_128204377del	GRCh37
NC_000003.10:g.129687065_129687067del	NCBI36
NG_029334.1:g.12656_12658del , LRG_295:g.12656_12658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.871+195_871+197del MANE Plus Clinical	ENSP00000417074.1:n.871+195_871+197del
ENST00000696466.1:c.1153+195_1153+197del	ENSP00000512647.1:n.1153+195_1153+197del
ENST00000341105.7:c.871+195_871+197del MANE Select	ENSP00000345681.2:n.871+195_871+197del
ENST00000341105.6:c.871+195_871+197del	ENSP00000345681.2:n.871+195_871+197del
ENST00000430265.6:c.871+195_871+197del	ENSP00000400259.2:n.871+195_871+197del
ENST00000487848.5:c.871+195_871+197del	ENSP00000417074.1:n.871+195_871+197del
NM_001145661.1:c.871+195_871+197del , LRG_295t1:c.871+195_871+197del	NP_001139133.1:n.871+195_871+197del
NM_001145662.1:c.871+195_871+197del	NP_001139134.1:n.871+195_871+197del
NM_032638.4:c.871+195_871+197del , LRG_295t2:c.871+195_871+197del	NP_116027.2:n.871+195_871+197del
NM_001145661.2:c.871+195_871+197del MANE Plus Clinical	NP_001139133.1:n.871+195_871+197del
NM_032638.5:c.871+195_871+197del MANE Select	NP_116027.2:n.871+195_871+197del