Canonical Allele Identifier: CA1502448393

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148280388A= , CM000666.2:g.148280388A=	GRCh38
NC_000004.11:g.149201540A= , CM000666.1:g.149201540A=	GRCh37
NC_000004.10:g.149420990A=	NCBI36
NG_013350.1:g.167133T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.1758-20271T= MANE Select	ENSP00000350815.3:n.1758-20271T=
ENST00000342437.8:c.1758-20271T=	ENSP00000343907.4:n.1758-20271T=
ENST00000344721.8:c.1758-20271T=	ENSP00000341390.4:n.1758-20271T=
ENST00000358102.7:c.1758-20271T=	ENSP00000350815.3:n.1758-20271T=
ENST00000504753.1:n.207-20271T=
ENST00000511528.1:c.1758-20271T=	ENSP00000421481.1:n.1758-20271T=
ENST00000512865.5:c.1758-20271T=	ENSP00000423510.1:n.1758-20271T=
ENST00000625323.2:c.1758-20271T=	ENSP00000486719.1:n.1758-20271T=
NM_000901.4:c.1758-20271T=	NP_000892.2:n.1758-20271T=
NM_001166104.1:c.1758-20271T=	NP_001159576.1:n.1758-20271T=
XM_011531975.1:c.1758-20271T=	XP_011530277.1:n.1758-20271T=
XM_011531976.1:c.1758-20271T=	XP_011530278.1:n.1758-20271T=
XM_011531977.1:c.1758-20271T=	XP_011530279.1:n.1758-20271T=
XM_011531978.1:c.1758-20271T=	XP_011530280.1:n.1758-20271T=
NM_001354819.1:c.1758-20271T=	NP_001341748.1:n.1758-20271T=
NR_148974.1:n.2121-20271T=
XM_011531978.2:c.1758-20271T=	XP_011530280.1:n.1758-20271T=
NM_000901.5:c.1758-20271T= MANE Select	NP_000892.2:n.1758-20271T=
NM_001166104.2:c.1758-20271T=	NP_001159576.1:n.1758-20271T=
NR_148974.2:n.2015-20271T=