Canonical Allele Identifier: CA1914712972

Gene: EGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62813974T= , CM000672.2:g.62813974T=	GRCh38
NC_000010.10:g.64573734T= , CM000672.1:g.64573734T=	GRCh37
NC_000010.9:g.64243740T=	NCBI36
NG_008936.2:g.110927A= , LRG_239:g.110927A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411732.4:c.514A=	ENSP00000387634.1:p.Met172=
ENST00000439032.6:c.1204A=	ENSP00000509775.1:n.1204A=
ENST00000637191.2:c.664A=	ENSP00000490154.2:p.Met222=
ENST00000690143.1:c.*596A=	ENSP00000510306.1:n.*596A=
ENST00000691610.1:c.703A=	ENSP00000509830.1:p.Met235=
ENST00000242480.4:c.664A= MANE Select	ENSP00000242480.3:p.Met222=
ENST00000411732.3:c.514A=	ENSP00000387634.1:p.Met172=
ENST00000639815.1:n.109-1012A=
ENST00000242480.3:c.664A=	ENSP00000242480.3:p.Met222=
ENST00000411732.2:c.514A=	ENSP00000387634.1:p.Met172=
ENST00000439032.4:c.664A=	ENSP00000402040.1:p.Met222=
NM_000399.3:c.664A= , LRG_239t1:c.664A=	NP_000390.2:p.Met222=
NM_001136177.1:c.664A=	NP_001129649.1:p.Met222=
NM_001136178.1:c.664A=	NP_001129650.1:p.Met222=
NM_001136179.1:c.514A=	NP_001129651.1:p.Met172=
XM_011539427.1:c.703A=	XP_011537729.1:p.Met235=
XM_011539428.1:c.514A=	XP_011537730.1:p.Met172=
XM_011539429.1:c.514A=	XP_011537731.1:p.Met172=
NM_000399.4:c.664A=	NP_000390.2:p.Met222=
NM_001136177.2:c.664A=	NP_001129649.1:p.Met222=
NM_001136179.2:c.514A=	NP_001129651.1:p.Met172=
NM_001321037.1:c.514A=	NP_001307966.1:p.Met172=
NM_000399.5:c.664A= MANE Select	NP_000390.2:p.Met222=
NM_001136177.3:c.664A=	NP_001129649.1:p.Met222=
NM_001136179.3:c.514A=	NP_001129651.1:p.Met172=
NM_001321037.2:c.514A=	NP_001307966.1:p.Met172=
NM_001136178.2:c.664A=	NP_001129650.1:p.Met222=