Canonical Allele Identifier: CA2578208397
Gene: NR3C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148436823_148436828del , CM000666.2:g.148436823_148436828del GRCh38
NC_000004.11:g.149357975_149357980del , CM000666.1:g.149357975_149357980del GRCh37
NC_000004.10:g.149577425_149577430del NCBI36
NG_013350.1:g.10695_10700del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.35_40del MANE Select ENSP00000350815.3:p.Gly12_Leu13del
ENST00000342437.8:c.35_40del ENSP00000343907.4:p.Gly12_Leu13del
ENST00000344721.8:c.35_40del ENSP00000341390.4:p.Gly12_Leu13del
ENST00000358102.7:c.35_40del ENSP00000350815.3:p.Gly12_Leu13del
ENST00000511528.1:c.35_40del ENSP00000421481.1:p.Gly12_Leu13del
ENST00000512865.5:c.35_40del ENSP00000423510.1:p.Gly12_Leu13del
ENST00000625323.2:c.35_40del ENSP00000486719.1:p.Gly12_Leu13del
NM_000901.4:c.35_40del NP_000892.2:p.Gly12_Leu13del
NM_001166104.1:c.35_40del NP_001159576.1:p.Gly12_Leu13del
XM_011531975.1:c.35_40del XP_011530277.1:p.Gly12_Leu13del
XM_011531976.1:c.35_40del XP_011530278.1:p.Gly12_Leu13del
XM_011531977.1:c.35_40del XP_011530279.1:p.Gly12_Leu13del
XM_011531978.1:c.35_40del XP_011530280.1:p.Gly12_Leu13del
NM_001354819.1:c.35_40del NP_001341748.1:p.Gly12_Leu13del
NR_148974.1:n.398_403del
XM_011531978.2:c.35_40del XP_011530280.1:p.Gly12_Leu13del
NM_000901.5:c.35_40del MANE Select NP_000892.2:p.Gly12_Leu13del
NM_001166104.2:c.35_40del NP_001159576.1:p.Gly12_Leu13del
NR_148974.2:n.292_297del