Canonical Allele Identifier: CA1914713065

Gene: EGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62814195G= , CM000672.2:g.62814195G=	GRCh38
NC_000010.10:g.64573955G= , CM000672.1:g.64573955G=	GRCh37
NC_000010.9:g.64243961G=	NCBI36
NG_008936.2:g.110706C= , LRG_239:g.110706C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411732.4:c.293C=	ENSP00000387634.1:p.Pro98=
ENST00000439032.6:c.983C=	ENSP00000509775.1:n.983C=
ENST00000637191.2:c.443C=	ENSP00000490154.2:p.Pro148=
ENST00000690143.1:c.*375C=	ENSP00000510306.1:n.*375C=
ENST00000691610.1:c.482C=	ENSP00000509830.1:p.Pro161=
ENST00000242480.4:c.443C= MANE Select	ENSP00000242480.3:p.Pro148=
ENST00000411732.3:c.293C=	ENSP00000387634.1:p.Pro98=
ENST00000639815.1:n.109-1233C=
ENST00000242480.3:c.443C=	ENSP00000242480.3:p.Pro148=
ENST00000411732.2:c.293C=	ENSP00000387634.1:p.Pro98=
ENST00000439032.4:c.443C=	ENSP00000402040.1:p.Pro148=
NM_000399.3:c.443C= , LRG_239t1:c.443C=	NP_000390.2:p.Pro148=
NM_001136177.1:c.443C=	NP_001129649.1:p.Pro148=
NM_001136178.1:c.443C=	NP_001129650.1:p.Pro148=
NM_001136179.1:c.293C=	NP_001129651.1:p.Pro98=
XM_011539427.1:c.482C=	XP_011537729.1:p.Pro161=
XM_011539428.1:c.293C=	XP_011537730.1:p.Pro98=
XM_011539429.1:c.293C=	XP_011537731.1:p.Pro98=
NM_000399.4:c.443C=	NP_000390.2:p.Pro148=
NM_001136177.2:c.443C=	NP_001129649.1:p.Pro148=
NM_001136179.2:c.293C=	NP_001129651.1:p.Pro98=
NM_001321037.1:c.293C=	NP_001307966.1:p.Pro98=
NM_000399.5:c.443C= MANE Select	NP_000390.2:p.Pro148=
NM_001136177.3:c.443C=	NP_001129649.1:p.Pro148=
NM_001136179.3:c.293C=	NP_001129651.1:p.Pro98=
NM_001321037.2:c.293C=	NP_001307966.1:p.Pro98=
NM_001136178.2:c.443C=	NP_001129650.1:p.Pro148=