Canonical Allele Identifier: CA2695212035

Gene: EGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62813709_62813710insGGC , CM000672.2:g.62813709_62813710insGGC	GRCh38
NC_000010.10:g.64573469_64573470insGGC , CM000672.1:g.64573469_64573470insGGC	GRCh37
NC_000010.9:g.64243475_64243476insGGC	NCBI36
NG_008936.2:g.111191_111192insGCC , LRG_239:g.111191_111192insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411732.4:c.778_779insGCC	ENSP00000387634.1:p.Tyr260delinsCysHis
ENST00000439032.6:c.1468_1469insGCC	ENSP00000509775.1:n.1468_1469insGCC
ENST00000637191.2:c.928_929insGCC	ENSP00000490154.2:p.Tyr310delinsCysHis
ENST00000690143.1:c.*860_*861insGCC	ENSP00000510306.1:n.*860_*861insGCC
ENST00000691610.1:c.967_968insGCC	ENSP00000509830.1:p.Tyr323delinsCysHis
ENST00000242480.4:c.928_929insGCC MANE Select	ENSP00000242480.3:p.Tyr310delinsCysHis
ENST00000411732.3:c.778_779insGCC	ENSP00000387634.1:p.Tyr260delinsCysHis
ENST00000639815.1:n.109-748_109-747insGCC
ENST00000242480.3:c.928_929insGCC	ENSP00000242480.3:p.Tyr310delinsCysHis
ENST00000411732.2:c.778_779insGCC	ENSP00000387634.1:p.Tyr260delinsCysHis
ENST00000439032.4:c.928_929insGCC	ENSP00000402040.1:p.Tyr310delinsCysHis
NM_000399.3:c.928_929insGCC , LRG_239t1:c.928_929insGCC	NP_000390.2:p.Tyr310delinsCysHis
NM_001136177.1:c.928_929insGCC	NP_001129649.1:p.Tyr310delinsCysHis
NM_001136178.1:c.928_929insGCC	NP_001129650.1:p.Tyr310delinsCysHis
NM_001136179.1:c.778_779insGCC	NP_001129651.1:p.Tyr260delinsCysHis
XM_011539427.1:c.967_968insGCC	XP_011537729.1:p.Tyr323delinsCysHis
XM_011539428.1:c.778_779insGCC	XP_011537730.1:p.Tyr260delinsCysHis
XM_011539429.1:c.778_779insGCC	XP_011537731.1:p.Tyr260delinsCysHis
NM_000399.4:c.928_929insGCC	NP_000390.2:p.Tyr310delinsCysHis
NM_001136177.2:c.928_929insGCC	NP_001129649.1:p.Tyr310delinsCysHis
NM_001136179.2:c.778_779insGCC	NP_001129651.1:p.Tyr260delinsCysHis
NM_001321037.1:c.778_779insGCC	NP_001307966.1:p.Tyr260delinsCysHis
NM_000399.5:c.928_929insGCC MANE Select	NP_000390.2:p.Tyr310delinsCysHis
NM_001136177.3:c.928_929insGCC	NP_001129649.1:p.Tyr310delinsCysHis
NM_001136179.3:c.778_779insGCC	NP_001129651.1:p.Tyr260delinsCysHis
NM_001321037.2:c.778_779insGCC	NP_001307966.1:p.Tyr260delinsCysHis
NM_001136178.2:c.928_929insGCC	NP_001129650.1:p.Tyr310delinsCysHis