Canonical Allele Identifier: CA1502380502

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152477G= , CM000666.2:g.148152477G=	GRCh38
NC_000004.11:g.149073628G= , CM000666.1:g.149073628G=	GRCh37
NC_000004.10:g.149293078G=	NCBI36
NG_013350.1:g.295045C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2502C= MANE Select	ENSP00000350815.3:p.Val834=
ENST00000342437.8:c.2015-32189C=	ENSP00000343907.4:n.2015-32189C=
ENST00000344721.8:c.2502C=	ENSP00000341390.4:p.Val834=
ENST00000358102.7:c.2502C=	ENSP00000350815.3:p.Val834=
ENST00000503174.1:n.431C=
ENST00000503313.1:n.699C=
ENST00000511528.1:c.2514C=	ENSP00000421481.1:p.Val838=
ENST00000512865.5:c.2151C=	ENSP00000423510.1:p.Val717=
ENST00000625323.2:c.2514C=	ENSP00000486719.1:p.Val838=
NM_000901.4:c.2502C=	NP_000892.2:p.Val834=
NM_001166104.1:c.2151C=	NP_001159576.1:p.Val717=
XM_011531975.1:c.2514C=	XP_011530277.1:p.Val838=
XM_011531976.1:c.2514C=	XP_011530278.1:p.Val838=
XM_011531977.1:c.2514C=	XP_011530279.1:p.Val838=
XM_011531978.1:c.2514C=	XP_011530280.1:p.Val838=
NM_001354819.1:c.2151C=	NP_001341748.1:p.Val717=
NR_148974.1:n.2378-32189C=
XM_011531978.2:c.2514C=	XP_011530280.1:p.Val838=
NM_000901.5:c.2502C= MANE Select	NP_000892.2:p.Val834=
NM_001166104.2:c.2151C=	NP_001159576.1:p.Val717=
NR_148974.2:n.2272-32189C=