Canonical Allele Identifier: CA1914713037

Gene: EGR2

Linked Data

• dbSNP Id: rs1842200708

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62814137_62814139del , CM000672.2:g.62814137_62814139del	GRCh38
NC_000010.10:g.64573897_64573899del , CM000672.1:g.64573897_64573899del	GRCh37
NC_000010.9:g.64243903_64243905del	NCBI36
NG_008936.2:g.110764_110766del , LRG_239:g.110764_110766del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411732.4:c.351_353del	ENSP00000387634.1:p.Pro118del
ENST00000439032.6:c.1041_1043del	ENSP00000509775.1:n.1041_1043del
ENST00000637191.2:c.501_503del	ENSP00000490154.2:p.Pro168del
ENST00000690143.1:c.*433_*435del	ENSP00000510306.1:n.*433_*435del
ENST00000691610.1:c.540_542del	ENSP00000509830.1:p.Pro181del
ENST00000242480.4:c.501_503del MANE Select	ENSP00000242480.3:p.Pro168del
ENST00000411732.3:c.351_353del	ENSP00000387634.1:p.Pro118del
ENST00000639815.1:n.109-1175_109-1173del
ENST00000242480.3:c.501_503del	ENSP00000242480.3:p.Pro168del
ENST00000411732.2:c.351_353del	ENSP00000387634.1:p.Pro118del
ENST00000439032.4:c.501_503del	ENSP00000402040.1:p.Pro168del
NM_000399.3:c.501_503del , LRG_239t1:c.501_503del	NP_000390.2:p.Pro168del
NM_001136177.1:c.501_503del	NP_001129649.1:p.Pro168del
NM_001136178.1:c.501_503del	NP_001129650.1:p.Pro168del
NM_001136179.1:c.351_353del	NP_001129651.1:p.Pro118del
XM_011539427.1:c.540_542del	XP_011537729.1:p.Pro181del
XM_011539428.1:c.351_353del	XP_011537730.1:p.Pro118del
XM_011539429.1:c.351_353del	XP_011537731.1:p.Pro118del
NM_000399.4:c.501_503del	NP_000390.2:p.Pro168del
NM_001136177.2:c.501_503del	NP_001129649.1:p.Pro168del
NM_001136179.2:c.351_353del	NP_001129651.1:p.Pro118del
NM_001321037.1:c.351_353del	NP_001307966.1:p.Pro118del
NM_000399.5:c.501_503del MANE Select	NP_000390.2:p.Pro168del
NM_001136177.3:c.501_503del	NP_001129649.1:p.Pro168del
NM_001136179.3:c.351_353del	NP_001129651.1:p.Pro118del
NM_001321037.2:c.351_353del	NP_001307966.1:p.Pro118del
NM_001136178.2:c.501_503del	NP_001129650.1:p.Pro168del