Canonical Allele Identifier: CA2672314049
Gene: NR3C2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148154903_148154912del , CM000666.2:g.148154903_148154912del GRCh38
NC_000004.11:g.149076054_149076063del , CM000666.1:g.149076054_149076063del GRCh37
NC_000004.10:g.149295504_149295513del NCBI36
NG_013350.1:g.292611_292620del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.2015-10_2015-1del MANE Select ENSP00000350815.3:n.2015-10_2015-1del
ENST00000342437.8:c.2015-34623_2015-34614del ENSP00000343907.4:n.2015-34623_2015-34614del
ENST00000344721.8:c.2015-10_2015-1del ENSP00000341390.4:n.2015-10_2015-1del
ENST00000358102.7:c.2015-10_2015-1del ENSP00000350815.3:n.2015-10_2015-1del
ENST00000503313.1:n.212-10_212-1del
ENST00000511528.1:c.2027-10_2027-1del ENSP00000421481.1:n.2027-10_2027-1del
ENST00000512865.5:c.2015-2298_2015-2289del ENSP00000423510.1:n.2015-2298_2015-2289del
ENST00000625323.2:c.2027-10_2027-1del ENSP00000486719.1:n.2027-10_2027-1del
NM_000901.4:c.2015-10_2015-1del NP_000892.2:n.2015-10_2015-1del
NM_001166104.1:c.2015-2298_2015-2289del NP_001159576.1:n.2015-2298_2015-2289del
XM_011531975.1:c.2027-10_2027-1del XP_011530277.1:n.2027-10_2027-1del
XM_011531976.1:c.2027-10_2027-1del XP_011530278.1:n.2027-10_2027-1del
XM_011531977.1:c.2027-10_2027-1del XP_011530279.1:n.2027-10_2027-1del
XM_011531978.1:c.2027-10_2027-1del XP_011530280.1:n.2027-10_2027-1del
NM_001354819.1:c.2015-2298_2015-2289del NP_001341748.1:n.2015-2298_2015-2289del
NR_148974.1:n.2378-34623_2378-34614del
XM_011531978.2:c.2027-10_2027-1del XP_011530280.1:n.2027-10_2027-1del
NM_000901.5:c.2015-10_2015-1del MANE Select NP_000892.2:n.2015-10_2015-1del
NM_001166104.2:c.2015-2298_2015-2289del NP_001159576.1:n.2015-2298_2015-2289del
NR_148974.2:n.2272-34623_2272-34614del