Canonical Allele Identifier: CA2832528909

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081410_148081412dup , CM000666.2:g.148081410_148081412dup	GRCh38
NC_000004.11:g.149002561_149002563dup , CM000666.1:g.149002561_149002563dup	GRCh37
NC_000004.10:g.149222011_149222013dup	NCBI36
NG_013350.1:g.366114_366116dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2891_2893dup MANE Select	ENSP00000350815.3:p.Ile964_Ser965insIle
ENST00000342437.8:c.*274_*276dup	ENSP00000343907.4:n.*274_*276dup
ENST00000344721.8:c.2891_2893dup	ENSP00000341390.4:p.Ile964_Ser965insIle
ENST00000358102.7:c.2891_2893dup	ENSP00000350815.3:p.Ile964_Ser965insIle
ENST00000511528.1:c.2903_2905dup	ENSP00000421481.1:p.Ile968_Ser969insIle
ENST00000512865.5:c.2540_2542dup	ENSP00000423510.1:p.Ile847_Ser848insIle
ENST00000625323.2:c.2903_2905dup	ENSP00000486719.1:p.Ile968_Ser969insIle
NM_000901.4:c.2891_2893dup	NP_000892.2:p.Ile964_Ser965insIle
NM_001166104.1:c.2540_2542dup	NP_001159576.1:p.Ile847_Ser848insIle
XM_011531975.1:c.2903_2905dup	XP_011530277.1:p.Ile968_Ser969insIle
XM_011531976.1:c.2903_2905dup	XP_011530278.1:p.Ile968_Ser969insIle
XM_011531977.1:c.2903_2905dup	XP_011530279.1:p.Ile968_Ser969insIle
NM_001354819.1:c.2540_2542dup	NP_001341748.1:p.Ile847_Ser848insIle
NR_148974.1:n.2758_2760dup
NM_000901.5:c.2891_2893dup MANE Select	NP_000892.2:p.Ile964_Ser965insIle
NM_001166104.2:c.2540_2542dup	NP_001159576.1:p.Ile847_Ser848insIle
NR_148974.2:n.2652_2654dup