Canonical Allele Identifier: CA2695203847

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152515dup , CM000666.2:g.148152515dup	GRCh38
NC_000004.11:g.149073666dup , CM000666.1:g.149073666dup	GRCh37
NC_000004.10:g.149293116dup	NCBI36
NG_013350.1:g.295007dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2464dup MANE Select	ENSP00000350815.3:p.Thr822AsnfsTer15
ENST00000342437.8:c.2015-32227dup	ENSP00000343907.4:n.2015-32227dup
ENST00000344721.8:c.2464dup	ENSP00000341390.4:p.Thr822AsnfsTer15
ENST00000358102.7:c.2464dup	ENSP00000350815.3:p.Thr822AsnfsTer15
ENST00000503174.1:n.393dup
ENST00000503313.1:n.661dup
ENST00000511528.1:c.2476dup	ENSP00000421481.1:p.Thr826AsnfsTer15
ENST00000512865.5:c.2113dup	ENSP00000423510.1:p.Thr705AsnfsTer15
ENST00000625323.2:c.2476dup	ENSP00000486719.1:p.Thr826AsnfsTer15
NM_000901.4:c.2464dup	NP_000892.2:p.Thr822AsnfsTer15
NM_001166104.1:c.2113dup	NP_001159576.1:p.Thr705AsnfsTer15
XM_011531975.1:c.2476dup	XP_011530277.1:p.Thr826AsnfsTer15
XM_011531976.1:c.2476dup	XP_011530278.1:p.Thr826AsnfsTer15
XM_011531977.1:c.2476dup	XP_011530279.1:p.Thr826AsnfsTer15
XM_011531978.1:c.2476dup	XP_011530280.1:p.Thr826AsnfsTer15
NM_001354819.1:c.2113dup	NP_001341748.1:p.Thr705AsnfsTer15
NR_148974.1:n.2378-32227dup
XM_011531978.2:c.2476dup	XP_011530280.1:p.Thr826AsnfsTer15
NM_000901.5:c.2464dup MANE Select	NP_000892.2:p.Thr822AsnfsTer15
NM_001166104.2:c.2113dup	NP_001159576.1:p.Thr705AsnfsTer15
NR_148974.2:n.2272-32227dup