Canonical Allele Identifier: CA1914713036
Gene: EGR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62814134_62814137delinsTGGC , CM000672.2:g.62814134_62814137delinsTGGC GRCh38
NC_000010.10:g.64573894_64573897delinsTGGC , CM000672.1:g.64573894_64573897delinsTGGC GRCh37
NC_000010.9:g.64243900_64243903delinsTGGC NCBI36
NG_008936.2:g.110764_110767delinsGCCA , LRG_239:g.110764_110767delinsGCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000411732.4:c.351_354delinsGCCA ENSP00000387634.1:p.Pro117=
ENST00000439032.6:c.1041_1044delinsGCCA ENSP00000509775.1:n.1041_1044delinsGCCA
ENST00000637191.2:c.501_504delinsGCCA ENSP00000490154.2:p.Pro167=
ENST00000690143.1:c.*433_*436delinsGCCA ENSP00000510306.1:n.*433_*436delinsGCCA
ENST00000691610.1:c.540_543delinsGCCA ENSP00000509830.1:p.Pro180=
ENST00000242480.4:c.501_504delinsGCCA MANE Select ENSP00000242480.3:p.Pro167=
ENST00000411732.3:c.351_354delinsGCCA ENSP00000387634.1:p.Pro117=
ENST00000639815.1:n.109-1175_109-1172delinsGCCA
ENST00000242480.3:c.501_504delinsGCCA ENSP00000242480.3:p.Pro167=
ENST00000411732.2:c.351_354delinsGCCA ENSP00000387634.1:p.Pro117=
ENST00000439032.4:c.501_504delinsGCCA ENSP00000402040.1:p.Pro167=
NM_000399.3:c.501_504delinsGCCA , LRG_239t1:c.501_504delinsGCCA NP_000390.2:p.Pro167=
NM_001136177.1:c.501_504delinsGCCA NP_001129649.1:p.Pro167=
NM_001136178.1:c.501_504delinsGCCA NP_001129650.1:p.Pro167=
NM_001136179.1:c.351_354delinsGCCA NP_001129651.1:p.Pro117=
XM_011539427.1:c.540_543delinsGCCA XP_011537729.1:p.Pro180=
XM_011539428.1:c.351_354delinsGCCA XP_011537730.1:p.Pro117=
XM_011539429.1:c.351_354delinsGCCA XP_011537731.1:p.Pro117=
NM_000399.4:c.501_504delinsGCCA NP_000390.2:p.Pro167=
NM_001136177.2:c.501_504delinsGCCA NP_001129649.1:p.Pro167=
NM_001136179.2:c.351_354delinsGCCA NP_001129651.1:p.Pro117=
NM_001321037.1:c.351_354delinsGCCA NP_001307966.1:p.Pro117=
NM_000399.5:c.501_504delinsGCCA MANE Select NP_000390.2:p.Pro167=
NM_001136177.3:c.501_504delinsGCCA NP_001129649.1:p.Pro167=
NM_001136179.3:c.351_354delinsGCCA NP_001129651.1:p.Pro117=
NM_001321037.2:c.351_354delinsGCCA NP_001307966.1:p.Pro117=
NM_001136178.2:c.501_504delinsGCCA NP_001129650.1:p.Pro167=