Canonical Allele Identifier: CA358425608

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149002598G>T (hg19) ; chr4:g.148081447G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081447G>T , CM000666.2:g.148081447G>T	GRCh38
NC_000004.11:g.149002598G>T , CM000666.1:g.149002598G>T	GRCh37
NC_000004.10:g.149222048G>T	NCBI36
NG_013350.1:g.366075C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2852C>A MANE Select	ENSP00000350815.3:p.Ala951Glu
ENST00000342437.8:c.*235C>A	ENSP00000343907.4:n.*235C>A
ENST00000344721.8:c.2852C>A	ENSP00000341390.4:p.Ala951Glu
ENST00000358102.7:c.2852C>A	ENSP00000350815.3:p.Ala951Glu
ENST00000511528.1:c.2864C>A	ENSP00000421481.1:p.Ala955Glu
ENST00000512865.5:c.2501C>A	ENSP00000423510.1:p.Ala834Glu
ENST00000625323.2:c.2864C>A	ENSP00000486719.1:p.Ala955Glu
NM_000901.4:c.2852C>A	NP_000892.2:p.Ala951Glu
NM_001166104.1:c.2501C>A	NP_001159576.1:p.Ala834Glu
XM_011531975.1:c.2864C>A	XP_011530277.1:p.Ala955Glu
XM_011531976.1:c.2864C>A	XP_011530278.1:p.Ala955Glu
XM_011531977.1:c.2864C>A	XP_011530279.1:p.Ala955Glu
NM_001354819.1:c.2501C>A	NP_001341748.1:p.Ala834Glu
NR_148974.1:n.2719C>A
NM_000901.5:c.2852C>A MANE Select	NP_000892.2:p.Ala951Glu
NM_001166104.2:c.2501C>A	NP_001159576.1:p.Ala834Glu
NR_148974.2:n.2613C>A