Canonical Allele Identifier: CA2672314033
Gene: NR3C2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148154811_148154812insTGGGG , CM000666.2:g.148154811_148154812insTGGGG GRCh38
NC_000004.11:g.149075962_149075963insTGGGG , CM000666.1:g.149075962_149075963insTGGGG GRCh37
NC_000004.10:g.149295412_149295413insTGGGG NCBI36
NG_013350.1:g.292710_292711insCCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.2104_2105insCCCCA MANE Select ENSP00000350815.3:p.Gln702ProfsTer?
ENST00000342437.8:c.2015-34524_2015-34523insCCCCA ENSP00000343907.4:n.2015-34524_2015-34523insCCCCA
ENST00000344721.8:c.2104_2105insCCCCA ENSP00000341390.4:p.Gln702ProfsTer?
ENST00000358102.7:c.2104_2105insCCCCA ENSP00000350815.3:p.Gln702ProfsTer?
ENST00000503174.1:n.33_34insCCCCA
ENST00000503313.1:n.301_302insCCCCA
ENST00000511528.1:c.2116_2117insCCCCA ENSP00000421481.1:p.Gln706ProfsTer?
ENST00000512865.5:c.2015-2199_2015-2198insCCCCA ENSP00000423510.1:n.2015-2199_2015-2198insCCCCA
ENST00000625323.2:c.2116_2117insCCCCA ENSP00000486719.1:p.Gln706ProfsTer?
NM_000901.4:c.2104_2105insCCCCA NP_000892.2:p.Gln702ProfsTer?
NM_001166104.1:c.2015-2199_2015-2198insCCCCA NP_001159576.1:n.2015-2199_2015-2198insCCCCA
XM_011531975.1:c.2116_2117insCCCCA XP_011530277.1:p.Gln706ProfsTer?
XM_011531976.1:c.2116_2117insCCCCA XP_011530278.1:p.Gln706ProfsTer?
XM_011531977.1:c.2116_2117insCCCCA XP_011530279.1:p.Gln706ProfsTer?
XM_011531978.1:c.2116_2117insCCCCA XP_011530280.1:p.Gln706ProfsTer?
NM_001354819.1:c.2015-2199_2015-2198insCCCCA NP_001341748.1:n.2015-2199_2015-2198insCCCCA
NR_148974.1:n.2378-34524_2378-34523insCCCCA
XM_011531978.2:c.2116_2117insCCCCA XP_011530280.1:p.Gln706ProfsTer?
NM_000901.5:c.2104_2105insCCCCA MANE Select NP_000892.2:p.Gln702ProfsTer?
NM_001166104.2:c.2015-2199_2015-2198insCCCCA NP_001159576.1:n.2015-2199_2015-2198insCCCCA
NR_148974.2:n.2272-34524_2272-34523insCCCCA