Canonical Allele Identifier: CA2672314025

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148154611-G-GTCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154611_148154612insTCAA , CM000666.2:g.148154611_148154612insTCAA	GRCh38
NC_000004.11:g.149075762_149075763insTCAA , CM000666.1:g.149075762_149075763insTCAA	GRCh37
NC_000004.10:g.149295212_149295213insTCAA	NCBI36
NG_013350.1:g.292910_292911insTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2304_2305insTTGA MANE Select	ENSP00000350815.3:p.Asn770ThrfsTer23
ENST00000342437.8:c.2015-34324_2015-34323insTTGA	ENSP00000343907.4:n.2015-34324_2015-34323insTTGA
ENST00000344721.8:c.2304_2305insTTGA	ENSP00000341390.4:p.Asn770ThrfsTer23
ENST00000358102.7:c.2304_2305insTTGA	ENSP00000350815.3:p.Asn770ThrfsTer23
ENST00000503174.1:n.233_234insTTGA
ENST00000503313.1:n.501_502insTTGA
ENST00000511528.1:c.2316_2317insTTGA	ENSP00000421481.1:p.Asn774ThrfsTer23
ENST00000512865.5:c.2015-1999_2015-1998insTTGA	ENSP00000423510.1:n.2015-1999_2015-1998insTTGA
ENST00000625323.2:c.2316_2317insTTGA	ENSP00000486719.1:p.Asn774ThrfsTer23
NM_000901.4:c.2304_2305insTTGA	NP_000892.2:p.Asn770ThrfsTer23
NM_001166104.1:c.2015-1999_2015-1998insTTGA	NP_001159576.1:n.2015-1999_2015-1998insTTGA
XM_011531975.1:c.2316_2317insTTGA	XP_011530277.1:p.Asn774ThrfsTer23
XM_011531976.1:c.2316_2317insTTGA	XP_011530278.1:p.Asn774ThrfsTer23
XM_011531977.1:c.2316_2317insTTGA	XP_011530279.1:p.Asn774ThrfsTer23
XM_011531978.1:c.2316_2317insTTGA	XP_011530280.1:p.Asn774ThrfsTer23
NM_001354819.1:c.2015-1999_2015-1998insTTGA	NP_001341748.1:n.2015-1999_2015-1998insTTGA
NR_148974.1:n.2378-34324_2378-34323insTTGA
XM_011531978.2:c.2316_2317insTTGA	XP_011530280.1:p.Asn774ThrfsTer23
NM_000901.5:c.2304_2305insTTGA MANE Select	NP_000892.2:p.Asn770ThrfsTer23
NM_001166104.2:c.2015-1999_2015-1998insTTGA	NP_001159576.1:n.2015-1999_2015-1998insTTGA
NR_148974.2:n.2272-34324_2272-34323insTTGA