Canonical Allele Identifier: CA1914712841

Gene: EGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62813686G= , CM000672.2:g.62813686G=	GRCh38
NC_000010.10:g.64573446G= , CM000672.1:g.64573446G=	GRCh37
NC_000010.9:g.64243452G=	NCBI36
NG_008936.2:g.111215C= , LRG_239:g.111215C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411732.4:c.802C=	ENSP00000387634.1:p.Arg268=
ENST00000439032.6:c.1492C=	ENSP00000509775.1:n.1492C=
ENST00000637191.2:c.952C=	ENSP00000490154.2:p.Arg318=
ENST00000690143.1:c.*884C=	ENSP00000510306.1:n.*884C=
ENST00000691610.1:c.991C=	ENSP00000509830.1:p.Arg331=
ENST00000242480.4:c.952C= MANE Select	ENSP00000242480.3:p.Arg318=
ENST00000411732.3:c.802C=	ENSP00000387634.1:p.Arg268=
ENST00000639815.1:n.109-724C=
ENST00000242480.3:c.952C=	ENSP00000242480.3:p.Arg318=
ENST00000411732.2:c.802C=	ENSP00000387634.1:p.Arg268=
ENST00000439032.4:c.952C=	ENSP00000402040.1:p.Arg318=
NM_000399.3:c.952C= , LRG_239t1:c.952C=	NP_000390.2:p.Arg318=
NM_001136177.1:c.952C=	NP_001129649.1:p.Arg318=
NM_001136178.1:c.952C=	NP_001129650.1:p.Arg318=
NM_001136179.1:c.802C=	NP_001129651.1:p.Arg268=
XM_011539427.1:c.991C=	XP_011537729.1:p.Arg331=
XM_011539428.1:c.802C=	XP_011537730.1:p.Arg268=
XM_011539429.1:c.802C=	XP_011537731.1:p.Arg268=
NM_000399.4:c.952C=	NP_000390.2:p.Arg318=
NM_001136177.2:c.952C=	NP_001129649.1:p.Arg318=
NM_001136179.2:c.802C=	NP_001129651.1:p.Arg268=
NM_001321037.1:c.802C=	NP_001307966.1:p.Arg268=
NM_000399.5:c.952C= MANE Select	NP_000390.2:p.Arg318=
NM_001136177.3:c.952C=	NP_001129649.1:p.Arg318=
NM_001136179.3:c.802C=	NP_001129651.1:p.Arg268=
NM_001321037.2:c.802C=	NP_001307966.1:p.Arg268=
NM_001136178.2:c.952C=	NP_001129650.1:p.Arg318=