Canonical Allele Identifier: CA377028097
Gene: EGR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62813640G>A , CM000672.2:g.62813640G>A GRCh38
NC_000010.10:g.64573400G>A , CM000672.1:g.64573400G>A GRCh37
NC_000010.9:g.64243406G>A NCBI36
NG_008936.2:g.111261C>T , LRG_239:g.111261C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000411732.4:c.848C>T ENSP00000387634.1:p.Thr283Met
ENST00000439032.6:c.1538C>T ENSP00000509775.1:n.1538C>T
ENST00000637191.2:c.998C>T ENSP00000490154.2:p.Thr333Met
ENST00000690143.1:c.*930C>T ENSP00000510306.1:n.*930C>T
ENST00000691610.1:c.1037C>T ENSP00000509830.1:p.Thr346Met
ENST00000242480.4:c.998C>T MANE Select ENSP00000242480.3:p.Thr333Met
ENST00000411732.3:c.848C>T ENSP00000387634.1:p.Thr283Met
ENST00000639815.1:n.109-678C>T
ENST00000242480.3:c.998C>T ENSP00000242480.3:p.Thr333Met
ENST00000411732.2:c.848C>T ENSP00000387634.1:p.Thr283Met
ENST00000439032.4:c.998C>T ENSP00000402040.1:p.Thr333Met
NM_000399.3:c.998C>T , LRG_239t1:c.998C>T NP_000390.2:p.Thr333Met
NM_001136177.1:c.998C>T NP_001129649.1:p.Thr333Met
NM_001136178.1:c.998C>T NP_001129650.1:p.Thr333Met
NM_001136179.1:c.848C>T NP_001129651.1:p.Thr283Met
XM_011539427.1:c.1037C>T XP_011537729.1:p.Thr346Met
XM_011539428.1:c.848C>T XP_011537730.1:p.Thr283Met
XM_011539429.1:c.848C>T XP_011537731.1:p.Thr283Met
NM_000399.4:c.998C>T NP_000390.2:p.Thr333Met
NM_001136177.2:c.998C>T NP_001129649.1:p.Thr333Met
NM_001136179.2:c.848C>T NP_001129651.1:p.Thr283Met
NM_001321037.1:c.848C>T NP_001307966.1:p.Thr283Met
NM_000399.5:c.998C>T MANE Select NP_000390.2:p.Thr333Met
NM_001136177.3:c.998C>T NP_001129649.1:p.Thr333Met
NM_001136179.3:c.848C>T NP_001129651.1:p.Thr283Met
NM_001321037.2:c.848C>T NP_001307966.1:p.Thr283Met
NM_001136178.2:c.998C>T NP_001129650.1:p.Thr333Met