Canonical Allele Identifier: CA1502333392

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154835_148154838delinsGGCT , CM000666.2:g.148154835_148154838delinsGGCT	GRCh38
NC_000004.11:g.149075986_149075989delinsGGCT , CM000666.1:g.149075986_149075989delinsGGCT	GRCh37
NC_000004.10:g.149295436_149295439delinsGGCT	NCBI36
NG_013350.1:g.292684_292687delinsAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2078_2081delinsAGCC MANE Select	ENSP00000350815.3:p.Gln693=
ENST00000342437.8:c.2015-34550_2015-34547delinsAGCC	ENSP00000343907.4:n.2015-34550_2015-34547delinsAGCC
ENST00000344721.8:c.2078_2081delinsAGCC	ENSP00000341390.4:p.Gln693=
ENST00000358102.7:c.2078_2081delinsAGCC	ENSP00000350815.3:p.Gln693=
ENST00000503174.1:n.7_10delinsAGCC
ENST00000503313.1:n.275_278delinsAGCC
ENST00000511528.1:c.2090_2093delinsAGCC	ENSP00000421481.1:p.Gln697=
ENST00000512865.5:c.2015-2225_2015-2222delinsAGCC	ENSP00000423510.1:n.2015-2225_2015-2222delinsAGCC
ENST00000625323.2:c.2090_2093delinsAGCC	ENSP00000486719.1:p.Gln697=
NM_000901.4:c.2078_2081delinsAGCC	NP_000892.2:p.Gln693=
NM_001166104.1:c.2015-2225_2015-2222delinsAGCC	NP_001159576.1:n.2015-2225_2015-2222delinsAGCC
XM_011531975.1:c.2090_2093delinsAGCC	XP_011530277.1:p.Gln697=
XM_011531976.1:c.2090_2093delinsAGCC	XP_011530278.1:p.Gln697=
XM_011531977.1:c.2090_2093delinsAGCC	XP_011530279.1:p.Gln697=
XM_011531978.1:c.2090_2093delinsAGCC	XP_011530280.1:p.Gln697=
NM_001354819.1:c.2015-2225_2015-2222delinsAGCC	NP_001341748.1:n.2015-2225_2015-2222delinsAGCC
NR_148974.1:n.2378-34550_2378-34547delinsAGCC
XM_011531978.2:c.2090_2093delinsAGCC	XP_011530280.1:p.Gln697=
NM_000901.5:c.2078_2081delinsAGCC MANE Select	NP_000892.2:p.Gln693=
NM_001166104.2:c.2015-2225_2015-2222delinsAGCC	NP_001159576.1:n.2015-2225_2015-2222delinsAGCC
NR_148974.2:n.2272-34550_2272-34547delinsAGCC