Canonical Allele Identifier: CA1914712941
Gene: EGR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62813901C= , CM000672.2:g.62813901C= GRCh38
NC_000010.10:g.64573661C= , CM000672.1:g.64573661C= GRCh37
NC_000010.9:g.64243667C= NCBI36
NG_008936.2:g.111000G= , LRG_239:g.111000G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000411732.4:c.587G= ENSP00000387634.1:p.Arg196=
ENST00000439032.6:c.1277G= ENSP00000509775.1:n.1277G=
ENST00000637191.2:c.737G= ENSP00000490154.2:p.Arg246=
ENST00000690143.1:c.*669G= ENSP00000510306.1:n.*669G=
ENST00000691610.1:c.776G= ENSP00000509830.1:p.Arg259=
ENST00000242480.4:c.737G= MANE Select ENSP00000242480.3:p.Arg246=
ENST00000411732.3:c.587G= ENSP00000387634.1:p.Arg196=
ENST00000639815.1:n.109-939G=
ENST00000242480.3:c.737G= ENSP00000242480.3:p.Arg246=
ENST00000411732.2:c.587G= ENSP00000387634.1:p.Arg196=
ENST00000439032.4:c.737G= ENSP00000402040.1:p.Arg246=
NM_000399.3:c.737G= , LRG_239t1:c.737G= NP_000390.2:p.Arg246=
NM_001136177.1:c.737G= NP_001129649.1:p.Arg246=
NM_001136178.1:c.737G= NP_001129650.1:p.Arg246=
NM_001136179.1:c.587G= NP_001129651.1:p.Arg196=
XM_011539427.1:c.776G= XP_011537729.1:p.Arg259=
XM_011539428.1:c.587G= XP_011537730.1:p.Arg196=
XM_011539429.1:c.587G= XP_011537731.1:p.Arg196=
NM_000399.4:c.737G= NP_000390.2:p.Arg246=
NM_001136177.2:c.737G= NP_001129649.1:p.Arg246=
NM_001136179.2:c.587G= NP_001129651.1:p.Arg196=
NM_001321037.1:c.587G= NP_001307966.1:p.Arg196=
NM_000399.5:c.737G= MANE Select NP_000390.2:p.Arg246=
NM_001136177.3:c.737G= NP_001129649.1:p.Arg246=
NM_001136179.3:c.587G= NP_001129651.1:p.Arg196=
NM_001321037.2:c.587G= NP_001307966.1:p.Arg196=
NM_001136178.2:c.737G= NP_001129650.1:p.Arg246=