Canonical Allele Identifier: CA1914713048
Gene: EGR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62814162G= , CM000672.2:g.62814162G= GRCh38
NC_000010.10:g.64573922G= , CM000672.1:g.64573922G= GRCh37
NC_000010.9:g.64243928G= NCBI36
NG_008936.2:g.110739C= , LRG_239:g.110739C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000411732.4:c.326C= ENSP00000387634.1:p.Pro109=
ENST00000439032.6:c.1016C= ENSP00000509775.1:n.1016C=
ENST00000637191.2:c.476C= ENSP00000490154.2:p.Pro159=
ENST00000690143.1:c.*408C= ENSP00000510306.1:n.*408C=
ENST00000691610.1:c.515C= ENSP00000509830.1:p.Pro172=
ENST00000242480.4:c.476C= MANE Select ENSP00000242480.3:p.Pro159=
ENST00000411732.3:c.326C= ENSP00000387634.1:p.Pro109=
ENST00000639815.1:n.109-1200C=
ENST00000242480.3:c.476C= ENSP00000242480.3:p.Pro159=
ENST00000411732.2:c.326C= ENSP00000387634.1:p.Pro109=
ENST00000439032.4:c.476C= ENSP00000402040.1:p.Pro159=
NM_000399.3:c.476C= , LRG_239t1:c.476C= NP_000390.2:p.Pro159=
NM_001136177.1:c.476C= NP_001129649.1:p.Pro159=
NM_001136178.1:c.476C= NP_001129650.1:p.Pro159=
NM_001136179.1:c.326C= NP_001129651.1:p.Pro109=
XM_011539427.1:c.515C= XP_011537729.1:p.Pro172=
XM_011539428.1:c.326C= XP_011537730.1:p.Pro109=
XM_011539429.1:c.326C= XP_011537731.1:p.Pro109=
NM_000399.4:c.476C= NP_000390.2:p.Pro159=
NM_001136177.2:c.476C= NP_001129649.1:p.Pro159=
NM_001136179.2:c.326C= NP_001129651.1:p.Pro109=
NM_001321037.1:c.326C= NP_001307966.1:p.Pro109=
NM_000399.5:c.476C= MANE Select NP_000390.2:p.Pro159=
NM_001136177.3:c.476C= NP_001129649.1:p.Pro159=
NM_001136179.3:c.326C= NP_001129651.1:p.Pro109=
NM_001321037.2:c.326C= NP_001307966.1:p.Pro109=
NM_001136178.2:c.476C= NP_001129650.1:p.Pro159=