Canonical Allele Identifier: CA1502331624

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081467G= , CM000666.2:g.148081467G=	GRCh38
NC_000004.11:g.149002618G= , CM000666.1:g.149002618G=	GRCh37
NC_000004.10:g.149222068G=	NCBI36
NG_013350.1:g.366055C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2832C= MANE Select	ENSP00000350815.3:p.Tyr944=
ENST00000342437.8:c.*215C=	ENSP00000343907.4:n.*215C=
ENST00000344721.8:c.2832C=	ENSP00000341390.4:p.Tyr944=
ENST00000358102.7:c.2832C=	ENSP00000350815.3:p.Tyr944=
ENST00000511528.1:c.2844C=	ENSP00000421481.1:p.Tyr948=
ENST00000512865.5:c.2481C=	ENSP00000423510.1:p.Tyr827=
ENST00000625323.2:c.2844C=	ENSP00000486719.1:p.Tyr948=
NM_000901.4:c.2832C=	NP_000892.2:p.Tyr944=
NM_001166104.1:c.2481C=	NP_001159576.1:p.Tyr827=
XM_011531975.1:c.2844C=	XP_011530277.1:p.Tyr948=
XM_011531976.1:c.2844C=	XP_011530278.1:p.Tyr948=
XM_011531977.1:c.2844C=	XP_011530279.1:p.Tyr948=
NM_001354819.1:c.2481C=	NP_001341748.1:p.Tyr827=
NR_148974.1:n.2699C=
NM_000901.5:c.2832C= MANE Select	NP_000892.2:p.Tyr944=
NM_001166104.2:c.2481C=	NP_001159576.1:p.Tyr827=
NR_148974.2:n.2593C=