Canonical Allele Identifier: CA5517225

Gene: EGR2

Linked Data

• ClinVar Variation Id: 702426
• ClinVar RCV Id: RCV000871512
• dbSNP Id: rs758589570
• ExAC: 10:64573597 T / A
• gnomAD v2: 10-64573597-T-A
• gnomAD v3: 10-62813837-T-A
• gnomAD v4: 10-62813837-T-A
• MyVariant Identifiers: chr10:g.64573597T>A (hg19) ; chr10:g.62813837T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62813837T>A , CM000672.2:g.62813837T>A	GRCh38
NC_000010.10:g.64573597T>A , CM000672.1:g.64573597T>A	GRCh37
NC_000010.9:g.64243603T>A	NCBI36
NG_008936.2:g.111064A>T , LRG_239:g.111064A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000411732.4:c.651A>T	ENSP00000387634.1:p.Thr217=
ENST00000439032.6:c.1341A>T	ENSP00000509775.1:n.1341A>T
ENST00000637191.2:c.801A>T	ENSP00000490154.2:p.Thr267=
ENST00000690143.1:c.*733A>T	ENSP00000510306.1:n.*733A>T
ENST00000691610.1:c.840A>T	ENSP00000509830.1:p.Thr280=
ENST00000242480.4:c.801A>T MANE Select	ENSP00000242480.3:p.Thr267=
ENST00000411732.3:c.651A>T	ENSP00000387634.1:p.Thr217=
ENST00000639815.1:n.109-875A>T
ENST00000242480.3:c.801A>T	ENSP00000242480.3:p.Thr267=
ENST00000411732.2:c.651A>T	ENSP00000387634.1:p.Thr217=
ENST00000439032.4:c.801A>T	ENSP00000402040.1:p.Thr267=
NM_000399.3:c.801A>T , LRG_239t1:c.801A>T	NP_000390.2:p.Thr267=
NM_001136177.1:c.801A>T	NP_001129649.1:p.Thr267=
NM_001136178.1:c.801A>T	NP_001129650.1:p.Thr267=
NM_001136179.1:c.651A>T	NP_001129651.1:p.Thr217=
XM_011539427.1:c.840A>T	XP_011537729.1:p.Thr280=
XM_011539428.1:c.651A>T	XP_011537730.1:p.Thr217=
XM_011539429.1:c.651A>T	XP_011537731.1:p.Thr217=
NM_000399.4:c.801A>T	NP_000390.2:p.Thr267=
NM_001136177.2:c.801A>T	NP_001129649.1:p.Thr267=
NM_001136179.2:c.651A>T	NP_001129651.1:p.Thr217=
NM_001321037.1:c.651A>T	NP_001307966.1:p.Thr217=
NM_000399.5:c.801A>T MANE Select	NP_000390.2:p.Thr267=
NM_001136177.3:c.801A>T	NP_001129649.1:p.Thr267=
NM_001136179.3:c.651A>T	NP_001129651.1:p.Thr217=
NM_001321037.2:c.651A>T	NP_001307966.1:p.Thr217=
NM_001136178.2:c.801A>T	NP_001129650.1:p.Thr267=