Canonical Allele Identifier: CA377028365

Gene: EGR2

Linked Data

• ClinVar Variation Id: 1766674
• ClinVar RCV Id: RCV002371705
• gnomAD v4: 10-62813703-G-C
• MyVariant Identifiers: chr10:g.64573463G>C (hg19) ; chr10:g.62813703G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62813703G>C , CM000672.2:g.62813703G>C	GRCh38
NC_000010.10:g.64573463G>C , CM000672.1:g.64573463G>C	GRCh37
NC_000010.9:g.64243469G>C	NCBI36
NG_008936.2:g.111198C>G , LRG_239:g.111198C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411732.4:c.785C>G	ENSP00000387634.1:p.Pro262Arg
ENST00000439032.6:c.1475C>G	ENSP00000509775.1:n.1475C>G
ENST00000637191.2:c.935C>G	ENSP00000490154.2:p.Pro312Arg
ENST00000690143.1:c.*867C>G	ENSP00000510306.1:n.*867C>G
ENST00000691610.1:c.974C>G	ENSP00000509830.1:p.Pro325Arg
ENST00000242480.4:c.935C>G MANE Select	ENSP00000242480.3:p.Pro312Arg
ENST00000411732.3:c.785C>G	ENSP00000387634.1:p.Pro262Arg
ENST00000639815.1:n.109-741C>G
ENST00000242480.3:c.935C>G	ENSP00000242480.3:p.Pro312Arg
ENST00000411732.2:c.785C>G	ENSP00000387634.1:p.Pro262Arg
ENST00000439032.4:c.935C>G	ENSP00000402040.1:p.Pro312Arg
NM_000399.3:c.935C>G , LRG_239t1:c.935C>G	NP_000390.2:p.Pro312Arg
NM_001136177.1:c.935C>G	NP_001129649.1:p.Pro312Arg
NM_001136178.1:c.935C>G	NP_001129650.1:p.Pro312Arg
NM_001136179.1:c.785C>G	NP_001129651.1:p.Pro262Arg
XM_011539427.1:c.974C>G	XP_011537729.1:p.Pro325Arg
XM_011539428.1:c.785C>G	XP_011537730.1:p.Pro262Arg
XM_011539429.1:c.785C>G	XP_011537731.1:p.Pro262Arg
NM_000399.4:c.935C>G	NP_000390.2:p.Pro312Arg
NM_001136177.2:c.935C>G	NP_001129649.1:p.Pro312Arg
NM_001136179.2:c.785C>G	NP_001129651.1:p.Pro262Arg
NM_001321037.1:c.785C>G	NP_001307966.1:p.Pro262Arg
NM_000399.5:c.935C>G MANE Select	NP_000390.2:p.Pro312Arg
NM_001136177.3:c.935C>G	NP_001129649.1:p.Pro312Arg
NM_001136179.3:c.785C>G	NP_001129651.1:p.Pro262Arg
NM_001321037.2:c.785C>G	NP_001307966.1:p.Pro262Arg
NM_001136178.2:c.935C>G	NP_001129650.1:p.Pro312Arg