Canonical Allele Identifier: CA1914712913
Gene: EGR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62813838G= , CM000672.2:g.62813838G= GRCh38
NC_000010.10:g.64573598G= , CM000672.1:g.64573598G= GRCh37
NC_000010.9:g.64243604G= NCBI36
NG_008936.2:g.111063C= , LRG_239:g.111063C=

Transcript Alleles

HGVS Amino-acid change
ENST00000411732.4:c.650C= ENSP00000387634.1:p.Thr217=
ENST00000439032.6:c.1340C= ENSP00000509775.1:n.1340C=
ENST00000637191.2:c.800C= ENSP00000490154.2:p.Thr267=
ENST00000690143.1:c.*732C= ENSP00000510306.1:n.*732C=
ENST00000691610.1:c.839C= ENSP00000509830.1:p.Thr280=
ENST00000242480.4:c.800C= MANE Select ENSP00000242480.3:p.Thr267=
ENST00000411732.3:c.650C= ENSP00000387634.1:p.Thr217=
ENST00000639815.1:n.109-876C=
ENST00000242480.3:c.800C= ENSP00000242480.3:p.Thr267=
ENST00000411732.2:c.650C= ENSP00000387634.1:p.Thr217=
ENST00000439032.4:c.800C= ENSP00000402040.1:p.Thr267=
NM_000399.3:c.800C= , LRG_239t1:c.800C= NP_000390.2:p.Thr267=
NM_001136177.1:c.800C= NP_001129649.1:p.Thr267=
NM_001136178.1:c.800C= NP_001129650.1:p.Thr267=
NM_001136179.1:c.650C= NP_001129651.1:p.Thr217=
XM_011539427.1:c.839C= XP_011537729.1:p.Thr280=
XM_011539428.1:c.650C= XP_011537730.1:p.Thr217=
XM_011539429.1:c.650C= XP_011537731.1:p.Thr217=
NM_000399.4:c.800C= NP_000390.2:p.Thr267=
NM_001136177.2:c.800C= NP_001129649.1:p.Thr267=
NM_001136179.2:c.650C= NP_001129651.1:p.Thr217=
NM_001321037.1:c.650C= NP_001307966.1:p.Thr217=
NM_000399.5:c.800C= MANE Select NP_000390.2:p.Thr267=
NM_001136177.3:c.800C= NP_001129649.1:p.Thr267=
NM_001136179.3:c.650C= NP_001129651.1:p.Thr217=
NM_001321037.2:c.650C= NP_001307966.1:p.Thr217=
NM_001136178.2:c.800C= NP_001129650.1:p.Thr267=