Canonical Allele Identifier: CA2672314038

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148154813-C-CGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154816_148154818dup , CM000666.2:g.148154816_148154818dup	GRCh38
NC_000004.11:g.149075967_149075969dup , CM000666.1:g.149075967_149075969dup	GRCh37
NC_000004.10:g.149295417_149295419dup	NCBI36
NG_013350.1:g.292706_292708dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2100_2102dup MANE Select	ENSP00000350815.3:p.Pro701_Gln702insPro
ENST00000342437.8:c.2015-34528_2015-34526dup	ENSP00000343907.4:n.2015-34528_2015-34526dup
ENST00000344721.8:c.2100_2102dup	ENSP00000341390.4:p.Pro701_Gln702insPro
ENST00000358102.7:c.2100_2102dup	ENSP00000350815.3:p.Pro701_Gln702insPro
ENST00000503174.1:n.29_31dup
ENST00000503313.1:n.297_299dup
ENST00000511528.1:c.2112_2114dup	ENSP00000421481.1:p.Pro705_Gln706insPro
ENST00000512865.5:c.2015-2203_2015-2201dup	ENSP00000423510.1:n.2015-2203_2015-2201dup
ENST00000625323.2:c.2112_2114dup	ENSP00000486719.1:p.Pro705_Gln706insPro
NM_000901.4:c.2100_2102dup	NP_000892.2:p.Pro701_Gln702insPro
NM_001166104.1:c.2015-2203_2015-2201dup	NP_001159576.1:n.2015-2203_2015-2201dup
XM_011531975.1:c.2112_2114dup	XP_011530277.1:p.Pro705_Gln706insPro
XM_011531976.1:c.2112_2114dup	XP_011530278.1:p.Pro705_Gln706insPro
XM_011531977.1:c.2112_2114dup	XP_011530279.1:p.Pro705_Gln706insPro
XM_011531978.1:c.2112_2114dup	XP_011530280.1:p.Pro705_Gln706insPro
NM_001354819.1:c.2015-2203_2015-2201dup	NP_001341748.1:n.2015-2203_2015-2201dup
NR_148974.1:n.2378-34528_2378-34526dup
XM_011531978.2:c.2112_2114dup	XP_011530280.1:p.Pro705_Gln706insPro
NM_000901.5:c.2100_2102dup MANE Select	NP_000892.2:p.Pro701_Gln702insPro
NM_001166104.2:c.2015-2203_2015-2201dup	NP_001159576.1:n.2015-2203_2015-2201dup
NR_148974.2:n.2272-34528_2272-34526dup