Canonical Allele Identifier: CA1400714586

Gene: GATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128481467_128481468delinsTG , CM000665.2:g.128481467_128481468delinsTG	GRCh38
NC_000003.11:g.128200310_128200311delinsTG , CM000665.1:g.128200310_128200311delinsTG	GRCh37
NC_000003.10:g.129683000_129683001delinsTG	NCBI36
NG_029334.1:g.16720_16721delinsCA , LRG_295:g.16720_16721delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000487848.6:c.1144-150_1144-149delinsCA MANE Plus Clinical	ENSP00000417074.1:n.1144-150_1144-149delinsCA
ENST00000696466.1:c.1426-150_1426-149delinsCA	ENSP00000512647.1:n.1426-150_1426-149delinsCA
ENST00000696672.1:c.127-158_127-157delinsCA	ENSP00000512796.1:n.127-158_127-157delinsCA
ENST00000341105.7:c.1144-150_1144-149delinsCA MANE Select	ENSP00000345681.2:n.1144-150_1144-149delinsCA
ENST00000341105.6:c.1144-150_1144-149delinsCA	ENSP00000345681.2:n.1144-150_1144-149delinsCA
ENST00000430265.6:c.1102-150_1102-149delinsCA	ENSP00000400259.2:n.1102-150_1102-149delinsCA
ENST00000487848.5:c.1144-150_1144-149delinsCA	ENSP00000417074.1:n.1144-150_1144-149delinsCA
ENST00000489987.1:n.261-150_261-149delinsCA
NM_001145661.1:c.1144-150_1144-149delinsCA , LRG_295t1:c.1144-150_1144-149delinsCA	NP_001139133.1:n.1144-150_1144-149delinsCA
NM_001145662.1:c.1102-150_1102-149delinsCA	NP_001139134.1:n.1102-150_1102-149delinsCA
NM_032638.4:c.1144-150_1144-149delinsCA , LRG_295t2:c.1144-150_1144-149delinsCA	NP_116027.2:n.1144-150_1144-149delinsCA
NM_001145661.2:c.1144-150_1144-149delinsCA MANE Plus Clinical	NP_001139133.1:n.1144-150_1144-149delinsCA
NM_032638.5:c.1144-150_1144-149delinsCA MANE Select	NP_116027.2:n.1144-150_1144-149delinsCA