Canonical Allele Identifier: CA1914712619
Gene: EGR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62813388G= , CM000672.2:g.62813388G= GRCh38
NC_000010.10:g.64573148G= , CM000672.1:g.64573148G= GRCh37
NC_000010.9:g.64243154G= NCBI36
NG_008936.2:g.111513C= , LRG_239:g.111513C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000411732.4:c.1100C= ENSP00000387634.1:p.Thr367=
ENST00000439032.6:c.1790C= ENSP00000509775.1:n.1790C=
ENST00000637191.2:c.1250C= ENSP00000490154.2:p.Thr417=
ENST00000690143.1:c.*1182C= ENSP00000510306.1:n.*1182C=
ENST00000691610.1:c.1289C= ENSP00000509830.1:p.Thr430=
ENST00000242480.4:c.1250C= MANE Select ENSP00000242480.3:p.Thr417=
ENST00000411732.3:c.1100C= ENSP00000387634.1:p.Thr367=
ENST00000639815.1:n.109-426C=
ENST00000242480.3:c.1250C= ENSP00000242480.3:p.Thr417=
ENST00000411732.2:c.1100C= ENSP00000387634.1:p.Thr367=
ENST00000439032.4:c.1250C= ENSP00000402040.1:p.Thr417=
NM_000399.3:c.1250C= , LRG_239t1:c.1250C= NP_000390.2:p.Thr417=
NM_001136177.1:c.1250C= NP_001129649.1:p.Thr417=
NM_001136178.1:c.1250C= NP_001129650.1:p.Thr417=
NM_001136179.1:c.1100C= NP_001129651.1:p.Thr367=
XM_011539427.1:c.1289C= XP_011537729.1:p.Thr430=
XM_011539428.1:c.1100C= XP_011537730.1:p.Thr367=
XM_011539429.1:c.1100C= XP_011537731.1:p.Thr367=
NM_000399.4:c.1250C= NP_000390.2:p.Thr417=
NM_001136177.2:c.1250C= NP_001129649.1:p.Thr417=
NM_001136179.2:c.1100C= NP_001129651.1:p.Thr367=
NM_001321037.1:c.1100C= NP_001307966.1:p.Thr367=
NM_000399.5:c.1250C= MANE Select NP_000390.2:p.Thr417=
NM_001136177.3:c.1250C= NP_001129649.1:p.Thr417=
NM_001136179.3:c.1100C= NP_001129651.1:p.Thr367=
NM_001321037.2:c.1100C= NP_001307966.1:p.Thr367=
NM_001136178.2:c.1250C= NP_001129650.1:p.Thr417=