Canonical Allele Identifier: CA1069289111
Gene: NR3C2 HGNC NCBI

Linked Data

dbSNP Id: rs1734278960

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148154818dup , CM000666.2:g.148154818dup GRCh38
NC_000004.11:g.149075969dup , CM000666.1:g.149075969dup GRCh37
NC_000004.10:g.149295419dup NCBI36
NG_013350.1:g.292708dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.2102dup MANE Select ENSP00000350815.3:p.Gln702AlafsTer?
ENST00000342437.8:c.2015-34526dup ENSP00000343907.4:n.2015-34526dup
ENST00000344721.8:c.2102dup ENSP00000341390.4:p.Gln702AlafsTer?
ENST00000358102.7:c.2102dup ENSP00000350815.3:p.Gln702AlafsTer?
ENST00000503174.1:n.31dup
ENST00000503313.1:n.299dup
ENST00000511528.1:c.2114dup ENSP00000421481.1:p.Gln706AlafsTer?
ENST00000512865.5:c.2015-2201dup ENSP00000423510.1:n.2015-2201dup
ENST00000625323.2:c.2114dup ENSP00000486719.1:p.Gln706AlafsTer?
NM_000901.4:c.2102dup NP_000892.2:p.Gln702AlafsTer?
NM_001166104.1:c.2015-2201dup NP_001159576.1:n.2015-2201dup
XM_011531975.1:c.2114dup XP_011530277.1:p.Gln706AlafsTer?
XM_011531976.1:c.2114dup XP_011530278.1:p.Gln706AlafsTer?
XM_011531977.1:c.2114dup XP_011530279.1:p.Gln706AlafsTer?
XM_011531978.1:c.2114dup XP_011530280.1:p.Gln706AlafsTer?
NM_001354819.1:c.2015-2201dup NP_001341748.1:n.2015-2201dup
NR_148974.1:n.2378-34526dup
XM_011531978.2:c.2114dup XP_011530280.1:p.Gln706AlafsTer?
NM_000901.5:c.2102dup MANE Select NP_000892.2:p.Gln702AlafsTer?
NM_001166104.2:c.2015-2201dup NP_001159576.1:n.2015-2201dup
NR_148974.2:n.2272-34526dup