Canonical Allele Identifier: CA2508071486

Gene: EGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62814854G>C , CM000672.2:g.62814854G>C	GRCh38
NC_000010.10:g.64574614G>C , CM000672.1:g.64574614G>C	GRCh37
NC_000010.9:g.64244620G>C	NCBI36
NG_008936.2:g.110047C>G , LRG_239:g.110047C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000411732.4:c.20-386C>G	ENSP00000387634.1:n.20-386C>G
ENST00000439032.6:c.710-386C>G	ENSP00000509775.1:n.710-386C>G
ENST00000637191.2:c.170-386C>G	ENSP00000490154.2:n.170-386C>G
ENST00000690143.1:c.*102-386C>G	ENSP00000510306.1:n.*102-386C>G
ENST00000691610.1:c.209-386C>G	ENSP00000509830.1:n.209-386C>G
ENST00000242480.4:c.170-386C>G MANE Select	ENSP00000242480.3:n.170-386C>G
ENST00000411732.3:c.20-386C>G	ENSP00000387634.1:n.20-386C>G
ENST00000637191.1:c.170-386C>G	ENSP00000490154.1:n.170-386C>G
ENST00000639815.1:n.108+1314C>G
ENST00000242480.3:c.170-386C>G	ENSP00000242480.3:n.170-386C>G
ENST00000411732.2:c.20-386C>G	ENSP00000387634.1:n.20-386C>G
ENST00000439032.4:c.170-386C>G	ENSP00000402040.1:n.170-386C>G
ENST00000493899.2:n.651-386C>G
NM_000399.3:c.170-386C>G , LRG_239t1:c.170-386C>G	NP_000390.2:n.170-386C>G
NM_001136177.1:c.170-386C>G	NP_001129649.1:n.170-386C>G
NM_001136178.1:c.170-386C>G	NP_001129650.1:n.170-386C>G
NM_001136179.1:c.20-386C>G	NP_001129651.1:n.20-386C>G
XM_011539427.1:c.209-386C>G	XP_011537729.1:n.209-386C>G
XM_011539428.1:c.20-386C>G	XP_011537730.1:n.20-386C>G
XM_011539429.1:c.20-386C>G	XP_011537731.1:n.20-386C>G
NM_000399.4:c.170-386C>G	NP_000390.2:n.170-386C>G
NM_001136177.2:c.170-386C>G	NP_001129649.1:n.170-386C>G
NM_001136179.2:c.20-386C>G	NP_001129651.1:n.20-386C>G
NM_001321037.1:c.20-386C>G	NP_001307966.1:n.20-386C>G
NM_000399.5:c.170-386C>G MANE Select	NP_000390.2:n.170-386C>G
NM_001136177.3:c.170-386C>G	NP_001129649.1:n.170-386C>G
NM_001136179.3:c.20-386C>G	NP_001129651.1:n.20-386C>G
NM_001321037.2:c.20-386C>G	NP_001307966.1:n.20-386C>G
NM_001136178.2:c.170-386C>G	NP_001129650.1:n.170-386C>G