Canonical Allele Identifier: CA1502329028

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148079934T= , CM000666.2:g.148079934T=	GRCh38
NC_000004.11:g.149001085T= , CM000666.1:g.149001085T=	GRCh37
NC_000004.10:g.149220535T=	NCBI36
NG_013350.1:g.367588A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000901.5:c.*1410A= MANE Select	NP_000892.2:n.*1410A=
ENST00000358102.8:c.*1410A= MANE Select	ENSP00000350815.3:n.*1410A=
NM_000901.4:c.*1410A=	NP_000892.2:n.*1410A=
NM_001166104.1:c.*1410A=	NP_001159576.1:n.*1410A=
NM_001166104.2:c.*1410A=	NP_001159576.1:n.*1410A=
NM_001354819.1:c.*1410A=	NP_001341748.1:n.*1410A=
NR_148974.1:n.4232A=
NR_148974.2:n.4126A=
ENST00000344721.8:c.*1410A=	ENSP00000341390.4:n.*1410A=
ENST00000358102.7:c.*1410A=	ENSP00000350815.3:n.*1410A=
ENST00000625323.2:c.*1410A=	ENSP00000486719.1:n.*1410A=
XM_011531975.1:c.*1410A=	XP_011530277.1:n.*1410A=
XM_011531976.1:c.*1410A=	XP_011530278.1:n.*1410A=
XM_011531977.1:c.*1410A=	XP_011530279.1:n.*1410A=