Canonical Allele Identifier: CA377027707

Gene: EGR2

Linked Data

• ClinVar Variation Id: 2827590
• ClinVar RCV Id: RCV003741912
• MyVariant Identifiers: chr10:g.64573292G>C (hg19) ; chr10:g.62813532G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62813532G>C , CM000672.2:g.62813532G>C	GRCh38
NC_000010.10:g.64573292G>C , CM000672.1:g.64573292G>C	GRCh37
NC_000010.9:g.64243298G>C	NCBI36
NG_008936.2:g.111369C>G , LRG_239:g.111369C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411732.4:c.956C>G	ENSP00000387634.1:p.Pro319Arg
ENST00000439032.6:c.1646C>G	ENSP00000509775.1:n.1646C>G
ENST00000637191.2:c.1106C>G	ENSP00000490154.2:p.Pro369Arg
ENST00000690143.1:c.*1038C>G	ENSP00000510306.1:n.*1038C>G
ENST00000691610.1:c.1145C>G	ENSP00000509830.1:p.Pro382Arg
ENST00000242480.4:c.1106C>G MANE Select	ENSP00000242480.3:p.Pro369Arg
ENST00000411732.3:c.956C>G	ENSP00000387634.1:p.Pro319Arg
ENST00000639815.1:n.109-570C>G
ENST00000242480.3:c.1106C>G	ENSP00000242480.3:p.Pro369Arg
ENST00000411732.2:c.956C>G	ENSP00000387634.1:p.Pro319Arg
ENST00000439032.4:c.1106C>G	ENSP00000402040.1:p.Pro369Arg
NM_000399.3:c.1106C>G , LRG_239t1:c.1106C>G	NP_000390.2:p.Pro369Arg
NM_001136177.1:c.1106C>G	NP_001129649.1:p.Pro369Arg
NM_001136178.1:c.1106C>G	NP_001129650.1:p.Pro369Arg
NM_001136179.1:c.956C>G	NP_001129651.1:p.Pro319Arg
XM_011539427.1:c.1145C>G	XP_011537729.1:p.Pro382Arg
XM_011539428.1:c.956C>G	XP_011537730.1:p.Pro319Arg
XM_011539429.1:c.956C>G	XP_011537731.1:p.Pro319Arg
NM_000399.4:c.1106C>G	NP_000390.2:p.Pro369Arg
NM_001136177.2:c.1106C>G	NP_001129649.1:p.Pro369Arg
NM_001136179.2:c.956C>G	NP_001129651.1:p.Pro319Arg
NM_001321037.1:c.956C>G	NP_001307966.1:p.Pro319Arg
NM_000399.5:c.1106C>G MANE Select	NP_000390.2:p.Pro369Arg
NM_001136177.3:c.1106C>G	NP_001129649.1:p.Pro369Arg
NM_001136179.3:c.956C>G	NP_001129651.1:p.Pro319Arg
NM_001321037.2:c.956C>G	NP_001307966.1:p.Pro319Arg
NM_001136178.2:c.1106C>G	NP_001129650.1:p.Pro369Arg