Canonical Allele Identifier: CA2672313796
Gene: NR3C2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148152353_148152354insTTTACAGATCTCTGGGAACTTAAAAA , CM000666.2:g.148152353_148152354insTTTACAGATCTCTGGGAACTTAAAAA GRCh38
NC_000004.11:g.149073504_149073505insTTTACAGATCTCTGGGAACTTAAAAA , CM000666.1:g.149073504_149073505insTTTACAGATCTCTGGGAACTTAAAAA GRCh37
NC_000004.10:g.149292954_149292955insTTTACAGATCTCTGGGAACTTAAAAA NCBI36
NG_013350.1:g.295175_295176insGTTCCCAGAGATCTGTAAATTTTTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.2510+122_2510+123insGTTCCCAGAGATCTGTAAATTTTTAA MANE Select ENSP00000350815.3:n.2510+122_2510+123insGTTCCCAGAGATCTGTAAATT...
ENST00000342437.8:c.2015-32059_2015-32058insGTTCCCAGAGATCTGTAAATTTTTAA ENSP00000343907.4:n.2015-32059_2015-32058insGTTCCCAGAGATCTGTA...
ENST00000344721.8:c.2510+122_2510+123insGTTCCCAGAGATCTGTAAATTTTTAA ENSP00000341390.4:n.2510+122_2510+123insGTTCCCAGAGATCTGTAAATT...
ENST00000358102.7:c.2510+122_2510+123insGTTCCCAGAGATCTGTAAATTTTTAA ENSP00000350815.3:n.2510+122_2510+123insGTTCCCAGAGATCTGTAAATT...
ENST00000503313.1:n.707+122_707+123insGTTCCCAGAGATCTGTAAATTTTTAA
ENST00000511528.1:c.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTTAA ENSP00000421481.1:n.2522+122_2522+123insGTTCCCAGAGATCTGTAAATT...
ENST00000512865.5:c.2159+122_2159+123insGTTCCCAGAGATCTGTAAATTTTTAA ENSP00000423510.1:n.2159+122_2159+123insGTTCCCAGAGATCTGTAAATT...
ENST00000625323.2:c.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTTAA ENSP00000486719.1:n.2522+122_2522+123insGTTCCCAGAGATCTGTAAATT...
NM_000901.4:c.2510+122_2510+123insGTTCCCAGAGATCTGTAAATTTTTAA NP_000892.2:n.2510+122_2510+123insGTTCCCAGAGATCTGTAAATTTTTAA
NM_001166104.1:c.2159+122_2159+123insGTTCCCAGAGATCTGTAAATTTTTAA NP_001159576.1:n.2159+122_2159+123insGTTCCCAGAGATCTGTAAATTTTT...
XM_011531975.1:c.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTTAA XP_011530277.1:n.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTT...
XM_011531976.1:c.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTTAA XP_011530278.1:n.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTT...
XM_011531977.1:c.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTTAA XP_011530279.1:n.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTT...
XM_011531978.1:c.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTTAA XP_011530280.1:n.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTT...
NM_001354819.1:c.2159+122_2159+123insGTTCCCAGAGATCTGTAAATTTTTAA NP_001341748.1:n.2159+122_2159+123insGTTCCCAGAGATCTGTAAATTTTT...
NR_148974.1:n.2378-32059_2378-32058insGTTCCCAGAGATCTGTAAATTTTTAA
XM_011531978.2:c.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTTAA XP_011530280.1:n.2522+122_2522+123insGTTCCCAGAGATCTGTAAATTTTT...
NM_000901.5:c.2510+122_2510+123insGTTCCCAGAGATCTGTAAATTTTTAA MANE Select NP_000892.2:n.2510+122_2510+123insGTTCCCAGAGATCTGTAAATTTTTAA
NM_001166104.2:c.2159+122_2159+123insGTTCCCAGAGATCTGTAAATTTTTAA NP_001159576.1:n.2159+122_2159+123insGTTCCCAGAGATCTGTAAATTTTT...
NR_148974.2:n.2272-32059_2272-32058insGTTCCCAGAGATCTGTAAATTTTTAA