Canonical Allele Identifier: CA1502331469

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081384T= , CM000666.2:g.148081384T=	GRCh38
NC_000004.11:g.149002535T= , CM000666.1:g.149002535T=	GRCh37
NC_000004.10:g.149221985T=	NCBI36
NG_013350.1:g.366138A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000901.5:c.2915A= MANE Select	NP_000892.2:p.Glu972=
ENST00000358102.8:c.2915A= MANE Select	ENSP00000350815.3:p.Glu972=
NM_000901.4:c.2915A=	NP_000892.2:p.Glu972=
NM_001166104.1:c.2564A=	NP_001159576.1:p.Glu855=
NM_001166104.2:c.2564A=	NP_001159576.1:p.Glu855=
NM_001354819.1:c.2564A=	NP_001341748.1:p.Glu855=
NR_148974.1:n.2782A=
NR_148974.2:n.2676A=
ENST00000342437.8:c.*298A=	ENSP00000343907.4:n.*298A=
ENST00000344721.8:c.2915A=	ENSP00000341390.4:p.Glu972=
ENST00000358102.7:c.2915A=	ENSP00000350815.3:p.Glu972=
ENST00000511528.1:c.2927A=	ENSP00000421481.1:p.Glu976=
ENST00000512865.5:c.2564A=	ENSP00000423510.1:p.Glu855=
ENST00000625323.2:c.2927A=	ENSP00000486719.1:p.Glu976=
XM_011531975.1:c.2927A=	XP_011530277.1:p.Glu976=
XM_011531976.1:c.2927A=	XP_011530278.1:p.Glu976=
XM_011531977.1:c.2927A=	XP_011530279.1:p.Glu976=