Canonical Allele Identifier: CA2667540671
Gene: GATA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128482166_128482168dup , CM000665.2:g.128482166_128482168dup GRCh38
NC_000003.11:g.128201009_128201011dup , CM000665.1:g.128201009_128201011dup GRCh37
NC_000003.10:g.129683699_129683701dup NCBI36
NG_029334.1:g.16020_16022dup , LRG_295:g.16020_16022dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.1018-224_1018-222dup MANE Plus Clinical ENSP00000417074.1:n.1018-224_1018-222dup
ENST00000696466.1:c.1300-224_1300-222dup ENSP00000512647.1:n.1300-224_1300-222dup
ENST00000341105.7:c.1018-224_1018-222dup MANE Select ENSP00000345681.2:n.1018-224_1018-222dup
ENST00000341105.6:c.1018-224_1018-222dup ENSP00000345681.2:n.1018-224_1018-222dup
ENST00000430265.6:c.1018-266_1018-264dup ENSP00000400259.2:n.1018-266_1018-264dup
ENST00000487848.5:c.1018-224_1018-222dup ENSP00000417074.1:n.1018-224_1018-222dup
NM_001145661.1:c.1018-224_1018-222dup , LRG_295t1:c.1018-224_1018-222dup NP_001139133.1:n.1018-224_1018-222dup
NM_001145662.1:c.1018-266_1018-264dup NP_001139134.1:n.1018-266_1018-264dup
NM_032638.4:c.1018-224_1018-222dup , LRG_295t2:c.1018-224_1018-222dup NP_116027.2:n.1018-224_1018-222dup
NM_001145661.2:c.1018-224_1018-222dup MANE Plus Clinical NP_001139133.1:n.1018-224_1018-222dup
NM_032638.5:c.1018-224_1018-222dup MANE Select NP_116027.2:n.1018-224_1018-222dup