Canonical Allele Identifier: CA2695212034

Gene: EGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62813491_62813492delinsAC , CM000672.2:g.62813491_62813492delinsAC	GRCh38
NC_000010.10:g.64573251_64573252delinsAC , CM000672.1:g.64573251_64573252delinsAC	GRCh37
NC_000010.9:g.64243257_64243258delinsAC	NCBI36
NG_008936.2:g.111409_111410delinsGT , LRG_239:g.111409_111410delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411732.4:c.996_997delinsGT	ENSP00000387634.1:p.Ser332_Asp333delinsArgTyr
ENST00000439032.6:c.1686_1687delinsGT	ENSP00000509775.1:n.1686_1687delinsGT
ENST00000637191.2:c.1146_1147delinsGT	ENSP00000490154.2:p.Ser382_Asp383delinsArgTyr
ENST00000690143.1:c.*1078_*1079delinsGT	ENSP00000510306.1:n.*1078_*1079delinsGT
ENST00000691610.1:c.1185_1186delinsGT	ENSP00000509830.1:p.Ser395_Asp396delinsArgTyr
ENST00000242480.4:c.1146_1147delinsGT MANE Select	ENSP00000242480.3:p.Ser382_Asp383delinsArgTyr
ENST00000411732.3:c.996_997delinsGT	ENSP00000387634.1:p.Ser332_Asp333delinsArgTyr
ENST00000639815.1:n.109-530_109-529delinsGT
ENST00000242480.3:c.1146_1147delinsGT	ENSP00000242480.3:p.Ser382_Asp383delinsArgTyr
ENST00000411732.2:c.996_997delinsGT	ENSP00000387634.1:p.Ser332_Asp333delinsArgTyr
ENST00000439032.4:c.1146_1147delinsGT	ENSP00000402040.1:p.Ser382_Asp383delinsArgTyr
NM_000399.3:c.1146_1147delinsGT , LRG_239t1:c.1146_1147delinsGT	NP_000390.2:p.Ser382_Asp383delinsArgTyr
NM_001136177.1:c.1146_1147delinsGT	NP_001129649.1:p.Ser382_Asp383delinsArgTyr
NM_001136178.1:c.1146_1147delinsGT	NP_001129650.1:p.Ser382_Asp383delinsArgTyr
NM_001136179.1:c.996_997delinsGT	NP_001129651.1:p.Ser332_Asp333delinsArgTyr
XM_011539427.1:c.1185_1186delinsGT	XP_011537729.1:p.Ser395_Asp396delinsArgTyr
XM_011539428.1:c.996_997delinsGT	XP_011537730.1:p.Ser332_Asp333delinsArgTyr
XM_011539429.1:c.996_997delinsGT	XP_011537731.1:p.Ser332_Asp333delinsArgTyr
NM_000399.4:c.1146_1147delinsGT	NP_000390.2:p.Ser382_Asp383delinsArgTyr
NM_001136177.2:c.1146_1147delinsGT	NP_001129649.1:p.Ser382_Asp383delinsArgTyr
NM_001136179.2:c.996_997delinsGT	NP_001129651.1:p.Ser332_Asp333delinsArgTyr
NM_001321037.1:c.996_997delinsGT	NP_001307966.1:p.Ser332_Asp333delinsArgTyr
NM_000399.5:c.1146_1147delinsGT MANE Select	NP_000390.2:p.Ser382_Asp383delinsArgTyr
NM_001136177.3:c.1146_1147delinsGT	NP_001129649.1:p.Ser382_Asp383delinsArgTyr
NM_001136179.3:c.996_997delinsGT	NP_001129651.1:p.Ser332_Asp333delinsArgTyr
NM_001321037.2:c.996_997delinsGT	NP_001307966.1:p.Ser332_Asp333delinsArgTyr
NM_001136178.2:c.1146_1147delinsGT	NP_001129650.1:p.Ser382_Asp383delinsArgTyr