Canonical Allele Identifier: CA2667540370

Gene: GATA2

Linked Data

• gnomAD v4: 3-128481469-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481469_128481470insGA , CM000665.2:g.128481469_128481470insGA	GRCh38
NC_000003.11:g.128200312_128200313insGA , CM000665.1:g.128200312_128200313insGA	GRCh37
NC_000003.10:g.129683002_129683003insGA	NCBI36
NG_029334.1:g.16718_16719insTC , LRG_295:g.16718_16719insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487848.6:c.1144-152_1144-151insTC MANE Plus Clinical	ENSP00000417074.1:n.1144-152_1144-151insTC
ENST00000696466.1:c.1426-152_1426-151insTC	ENSP00000512647.1:n.1426-152_1426-151insTC
ENST00000696672.1:c.127-160_127-159insTC	ENSP00000512796.1:n.127-160_127-159insTC
ENST00000341105.7:c.1144-152_1144-151insTC MANE Select	ENSP00000345681.2:n.1144-152_1144-151insTC
ENST00000341105.6:c.1144-152_1144-151insTC	ENSP00000345681.2:n.1144-152_1144-151insTC
ENST00000430265.6:c.1102-152_1102-151insTC	ENSP00000400259.2:n.1102-152_1102-151insTC
ENST00000487848.5:c.1144-152_1144-151insTC	ENSP00000417074.1:n.1144-152_1144-151insTC
ENST00000489987.1:n.261-152_261-151insTC
NM_001145661.1:c.1144-152_1144-151insTC , LRG_295t1:c.1144-152_1144-151insTC	NP_001139133.1:n.1144-152_1144-151insTC
NM_001145662.1:c.1102-152_1102-151insTC	NP_001139134.1:n.1102-152_1102-151insTC
NM_032638.4:c.1144-152_1144-151insTC , LRG_295t2:c.1144-152_1144-151insTC	NP_116027.2:n.1144-152_1144-151insTC
NM_001145661.2:c.1144-152_1144-151insTC MANE Plus Clinical	NP_001139133.1:n.1144-152_1144-151insTC
NM_032638.5:c.1144-152_1144-151insTC MANE Select	NP_116027.2:n.1144-152_1144-151insTC