Canonical Allele Identifier: CA1502331406

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081366G= , CM000666.2:g.148081366G=	GRCh38
NC_000004.11:g.149002517G= , CM000666.1:g.149002517G=	GRCh37
NC_000004.10:g.149221967G=	NCBI36
NG_013350.1:g.366156C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2933C= MANE Select	ENSP00000350815.3:p.Pro978=
ENST00000342437.8:c.*316C=	ENSP00000343907.4:n.*316C=
ENST00000344721.8:c.2933C=	ENSP00000341390.4:p.Pro978=
ENST00000358102.7:c.2933C=	ENSP00000350815.3:p.Pro978=
ENST00000511528.1:c.2945C=	ENSP00000421481.1:p.Pro982=
ENST00000512865.5:c.2582C=	ENSP00000423510.1:p.Pro861=
ENST00000625323.2:c.2945C=	ENSP00000486719.1:p.Pro982=
NM_000901.4:c.2933C=	NP_000892.2:p.Pro978=
NM_001166104.1:c.2582C=	NP_001159576.1:p.Pro861=
XM_011531975.1:c.2945C=	XP_011530277.1:p.Pro982=
XM_011531976.1:c.2945C=	XP_011530278.1:p.Pro982=
XM_011531977.1:c.2945C=	XP_011530279.1:p.Pro982=
NM_001354819.1:c.2582C=	NP_001341748.1:p.Pro861=
NR_148974.1:n.2800C=
NM_000901.5:c.2933C= MANE Select	NP_000892.2:p.Pro978=
NM_001166104.2:c.2582C=	NP_001159576.1:p.Pro861=
NR_148974.2:n.2694C=