Canonical Allele Identifier: CA2672312845

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148081283-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081286_148081288del , CM000666.2:g.148081286_148081288del	GRCh38
NC_000004.11:g.149002437_149002439del , CM000666.1:g.149002437_149002439del	GRCh37
NC_000004.10:g.149221887_149221889del	NCBI36
NG_013350.1:g.366236_366238del

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.*58_*60del MANE Select	ENSP00000350815.3:n.*58_*60del
ENST00000342437.8:c.*396_*398del	ENSP00000343907.4:n.*396_*398del
ENST00000344721.8:c.*58_*60del	ENSP00000341390.4:n.*58_*60del
ENST00000358102.7:c.*58_*60del	ENSP00000350815.3:n.*58_*60del
ENST00000512865.5:c.*58_*60del	ENSP00000423510.1:n.*58_*60del
ENST00000625323.2:c.*58_*60del	ENSP00000486719.1:n.*58_*60del
NM_000901.4:c.*58_*60del	NP_000892.2:n.*58_*60del
NM_001166104.1:c.*58_*60del	NP_001159576.1:n.*58_*60del
XM_011531975.1:c.*58_*60del	XP_011530277.1:n.*58_*60del
XM_011531976.1:c.*58_*60del	XP_011530278.1:n.*58_*60del
XM_011531977.1:c.*58_*60del	XP_011530279.1:n.*58_*60del
NM_001354819.1:c.*58_*60del	NP_001341748.1:n.*58_*60del
NR_148974.1:n.2880_2882del
NM_000901.5:c.*58_*60del MANE Select	NP_000892.2:n.*58_*60del
NM_001166104.2:c.*58_*60del	NP_001159576.1:n.*58_*60del
NR_148974.2:n.2774_2776del