Canonical Allele Identifier: CA1502380514

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152521T= , CM000666.2:g.148152521T=	GRCh38
NC_000004.11:g.149073672T= , CM000666.1:g.149073672T=	GRCh37
NC_000004.10:g.149293122T=	NCBI36
NG_013350.1:g.295001A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2458A= MANE Select	ENSP00000350815.3:p.Lys820=
ENST00000342437.8:c.2015-32233A=	ENSP00000343907.4:n.2015-32233A=
ENST00000344721.8:c.2458A=	ENSP00000341390.4:p.Lys820=
ENST00000358102.7:c.2458A=	ENSP00000350815.3:p.Lys820=
ENST00000503174.1:n.387A=
ENST00000503313.1:n.655A=
ENST00000511528.1:c.2470A=	ENSP00000421481.1:p.Lys824=
ENST00000512865.5:c.2107A=	ENSP00000423510.1:p.Lys703=
ENST00000625323.2:c.2470A=	ENSP00000486719.1:p.Lys824=
NM_000901.4:c.2458A=	NP_000892.2:p.Lys820=
NM_001166104.1:c.2107A=	NP_001159576.1:p.Lys703=
XM_011531975.1:c.2470A=	XP_011530277.1:p.Lys824=
XM_011531976.1:c.2470A=	XP_011530278.1:p.Lys824=
XM_011531977.1:c.2470A=	XP_011530279.1:p.Lys824=
XM_011531978.1:c.2470A=	XP_011530280.1:p.Lys824=
NM_001354819.1:c.2107A=	NP_001341748.1:p.Lys703=
NR_148974.1:n.2378-32233A=
XM_011531978.2:c.2470A=	XP_011530280.1:p.Lys824=
NM_000901.5:c.2458A= MANE Select	NP_000892.2:p.Lys820=
NM_001166104.2:c.2107A=	NP_001159576.1:p.Lys703=
NR_148974.2:n.2272-32233A=