Canonical Allele Identifier: CA5517269

Gene: EGR2

Linked Data

• ClinVar Variation Id: 2887451
• ClinVar RCV Id: RCV003742570
• dbSNP Id: rs756375039
• ExAC: 10:64573897 C / T
• gnomAD v2: 10-64573897-C-T
• gnomAD v3: 10-62814137-C-T
• gnomAD v4: 10-62814137-C-T
• COSMIC: COSM3375503
• MyVariant Identifiers: chr10:g.64573897C>T (hg19) ; chr10:g.62814137C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62814137C>T , CM000672.2:g.62814137C>T	GRCh38
NC_000010.10:g.64573897C>T , CM000672.1:g.64573897C>T	GRCh37
NC_000010.9:g.64243903C>T	NCBI36
NG_008936.2:g.110764G>A , LRG_239:g.110764G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411732.4:c.351G>A	ENSP00000387634.1:p.Pro117=
ENST00000439032.6:c.1041G>A	ENSP00000509775.1:n.1041G>A
ENST00000637191.2:c.501G>A	ENSP00000490154.2:p.Pro167=
ENST00000690143.1:c.*433G>A	ENSP00000510306.1:n.*433G>A
ENST00000691610.1:c.540G>A	ENSP00000509830.1:p.Pro180=
ENST00000242480.4:c.501G>A MANE Select	ENSP00000242480.3:p.Pro167=
ENST00000411732.3:c.351G>A	ENSP00000387634.1:p.Pro117=
ENST00000639815.1:n.109-1175G>A
ENST00000242480.3:c.501G>A	ENSP00000242480.3:p.Pro167=
ENST00000411732.2:c.351G>A	ENSP00000387634.1:p.Pro117=
ENST00000439032.4:c.501G>A	ENSP00000402040.1:p.Pro167=
NM_000399.3:c.501G>A , LRG_239t1:c.501G>A	NP_000390.2:p.Pro167=
NM_001136177.1:c.501G>A	NP_001129649.1:p.Pro167=
NM_001136178.1:c.501G>A	NP_001129650.1:p.Pro167=
NM_001136179.1:c.351G>A	NP_001129651.1:p.Pro117=
XM_011539427.1:c.540G>A	XP_011537729.1:p.Pro180=
XM_011539428.1:c.351G>A	XP_011537730.1:p.Pro117=
XM_011539429.1:c.351G>A	XP_011537731.1:p.Pro117=
NM_000399.4:c.501G>A	NP_000390.2:p.Pro167=
NM_001136177.2:c.501G>A	NP_001129649.1:p.Pro167=
NM_001136179.2:c.351G>A	NP_001129651.1:p.Pro117=
NM_001321037.1:c.351G>A	NP_001307966.1:p.Pro117=
NM_000399.5:c.501G>A MANE Select	NP_000390.2:p.Pro167=
NM_001136177.3:c.501G>A	NP_001129649.1:p.Pro167=
NM_001136179.3:c.351G>A	NP_001129651.1:p.Pro117=
NM_001321037.2:c.351G>A	NP_001307966.1:p.Pro117=
NM_001136178.2:c.501G>A	NP_001129650.1:p.Pro167=