Canonical Allele Identifier: CA2672314012

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148154522-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154523dup , CM000666.2:g.148154523dup	GRCh38
NC_000004.11:g.149075674dup , CM000666.1:g.149075674dup	GRCh37
NC_000004.10:g.149295124dup	NCBI36
NG_013350.1:g.292999dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2365+28dup MANE Select	ENSP00000350815.3:n.2365+28dup
ENST00000342437.8:c.2015-34235dup	ENSP00000343907.4:n.2015-34235dup
ENST00000344721.8:c.2365+28dup	ENSP00000341390.4:n.2365+28dup
ENST00000358102.7:c.2365+28dup	ENSP00000350815.3:n.2365+28dup
ENST00000503174.1:n.294+28dup
ENST00000503313.1:n.562+28dup
ENST00000511528.1:c.2377+28dup	ENSP00000421481.1:n.2377+28dup
ENST00000512865.5:c.2015-1910dup	ENSP00000423510.1:n.2015-1910dup
ENST00000625323.2:c.2377+28dup	ENSP00000486719.1:n.2377+28dup
NM_000901.4:c.2365+28dup	NP_000892.2:n.2365+28dup
NM_001166104.1:c.2015-1910dup	NP_001159576.1:n.2015-1910dup
XM_011531975.1:c.2377+28dup	XP_011530277.1:n.2377+28dup
XM_011531976.1:c.2377+28dup	XP_011530278.1:n.2377+28dup
XM_011531977.1:c.2377+28dup	XP_011530279.1:n.2377+28dup
XM_011531978.1:c.2377+28dup	XP_011530280.1:n.2377+28dup
NM_001354819.1:c.2015-1910dup	NP_001341748.1:n.2015-1910dup
NR_148974.1:n.2378-34235dup
XM_011531978.2:c.2377+28dup	XP_011530280.1:n.2377+28dup
NM_000901.5:c.2365+28dup MANE Select	NP_000892.2:n.2365+28dup
NM_001166104.2:c.2015-1910dup	NP_001159576.1:n.2015-1910dup
NR_148974.2:n.2272-34235dup