Canonical Allele Identifier: CA3100109
Gene: NR3C2 HGNC NCBI

Linked Data

dbSNP Id: rs756113767

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148152631_148152634del , CM000666.2:g.148152631_148152634del GRCh38
NC_000004.11:g.149073782_149073785del , CM000666.1:g.149073782_149073785del GRCh37
NC_000004.10:g.149293232_149293235del NCBI36
NG_013350.1:g.294891_294894del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.2366-18_2366-15del MANE Select ENSP00000350815.3:n.2366-18_2366-15del
ENST00000342437.8:c.2015-32343_2015-32340del ENSP00000343907.4:n.2015-32343_2015-32340del
ENST00000344721.8:c.2366-18_2366-15del ENSP00000341390.4:n.2366-18_2366-15del
ENST00000358102.7:c.2366-18_2366-15del ENSP00000350815.3:n.2366-18_2366-15del
ENST00000503174.1:n.295-18_295-15del
ENST00000503313.1:n.563-18_563-15del
ENST00000511528.1:c.2378-18_2378-15del ENSP00000421481.1:n.2378-18_2378-15del
ENST00000512865.5:c.2015-18_2015-15del ENSP00000423510.1:n.2015-18_2015-15del
ENST00000625323.2:c.2378-18_2378-15del ENSP00000486719.1:n.2378-18_2378-15del
NM_000901.4:c.2366-18_2366-15del NP_000892.2:n.2366-18_2366-15del
NM_001166104.1:c.2015-18_2015-15del NP_001159576.1:n.2015-18_2015-15del
XM_011531975.1:c.2378-18_2378-15del XP_011530277.1:n.2378-18_2378-15del
XM_011531976.1:c.2378-18_2378-15del XP_011530278.1:n.2378-18_2378-15del
XM_011531977.1:c.2378-18_2378-15del XP_011530279.1:n.2378-18_2378-15del
XM_011531978.1:c.2378-18_2378-15del XP_011530280.1:n.2378-18_2378-15del
NM_001354819.1:c.2015-18_2015-15del NP_001341748.1:n.2015-18_2015-15del
NR_148974.1:n.2378-32343_2378-32340del
XM_011531978.2:c.2378-18_2378-15del XP_011530280.1:n.2378-18_2378-15del
NM_000901.5:c.2366-18_2366-15del MANE Select NP_000892.2:n.2366-18_2366-15del
NM_001166104.2:c.2015-18_2015-15del NP_001159576.1:n.2015-18_2015-15del
NR_148974.2:n.2272-32343_2272-32340del