Canonical Allele Identifier: CA1914712585

Gene: EGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62813361C= , CM000672.2:g.62813361C=	GRCh38
NC_000010.10:g.64573121C= , CM000672.1:g.64573121C=	GRCh37
NC_000010.9:g.64243127C=	NCBI36
NG_008936.2:g.111540G= , LRG_239:g.111540G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411732.4:c.1127G=	ENSP00000387634.1:p.Arg376=
ENST00000439032.6:c.1817G=	ENSP00000509775.1:n.1817G=
ENST00000637191.2:c.1277G=	ENSP00000490154.2:p.Arg426=
ENST00000690143.1:c.*1209G=	ENSP00000510306.1:n.*1209G=
ENST00000691610.1:c.1316G=	ENSP00000509830.1:p.Arg439=
ENST00000242480.4:c.1277G= MANE Select	ENSP00000242480.3:p.Arg426=
ENST00000411732.3:c.1127G=	ENSP00000387634.1:p.Arg376=
ENST00000639815.1:n.109-399G=
ENST00000242480.3:c.1277G=	ENSP00000242480.3:p.Arg426=
ENST00000411732.2:c.1127G=	ENSP00000387634.1:p.Arg376=
ENST00000439032.4:c.1277G=	ENSP00000402040.1:p.Arg426=
NM_000399.3:c.1277G= , LRG_239t1:c.1277G=	NP_000390.2:p.Arg426=
NM_001136177.1:c.1277G=	NP_001129649.1:p.Arg426=
NM_001136178.1:c.1277G=	NP_001129650.1:p.Arg426=
NM_001136179.1:c.1127G=	NP_001129651.1:p.Arg376=
XM_011539427.1:c.1316G=	XP_011537729.1:p.Arg439=
XM_011539428.1:c.1127G=	XP_011537730.1:p.Arg376=
XM_011539429.1:c.1127G=	XP_011537731.1:p.Arg376=
NM_000399.4:c.1277G=	NP_000390.2:p.Arg426=
NM_001136177.2:c.1277G=	NP_001129649.1:p.Arg426=
NM_001136179.2:c.1127G=	NP_001129651.1:p.Arg376=
NM_001321037.1:c.1127G=	NP_001307966.1:p.Arg376=
NM_000399.5:c.1277G= MANE Select	NP_000390.2:p.Arg426=
NM_001136177.3:c.1277G=	NP_001129649.1:p.Arg426=
NM_001136179.3:c.1127G=	NP_001129651.1:p.Arg376=
NM_001321037.2:c.1127G=	NP_001307966.1:p.Arg376=
NM_001136178.2:c.1277G=	NP_001129650.1:p.Arg426=