Canonical Allele Identifier: CA358425870

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149073705G>T (hg19) ; chr4:g.148152554G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152554G>T , CM000666.2:g.148152554G>T	GRCh38
NC_000004.11:g.149073705G>T , CM000666.1:g.149073705G>T	GRCh37
NC_000004.10:g.149293155G>T	NCBI36
NG_013350.1:g.294968C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2425C>A MANE Select	ENSP00000350815.3:p.Leu809Ile
ENST00000342437.8:c.2015-32266C>A	ENSP00000343907.4:n.2015-32266C>A
ENST00000344721.8:c.2425C>A	ENSP00000341390.4:p.Leu809Ile
ENST00000358102.7:c.2425C>A	ENSP00000350815.3:p.Leu809Ile
ENST00000503174.1:n.354C>A
ENST00000503313.1:n.622C>A
ENST00000511528.1:c.2437C>A	ENSP00000421481.1:p.Leu813Ile
ENST00000512865.5:c.2074C>A	ENSP00000423510.1:p.Leu692Ile
ENST00000625323.2:c.2437C>A	ENSP00000486719.1:p.Leu813Ile
NM_000901.4:c.2425C>A	NP_000892.2:p.Leu809Ile
NM_001166104.1:c.2074C>A	NP_001159576.1:p.Leu692Ile
XM_011531975.1:c.2437C>A	XP_011530277.1:p.Leu813Ile
XM_011531976.1:c.2437C>A	XP_011530278.1:p.Leu813Ile
XM_011531977.1:c.2437C>A	XP_011530279.1:p.Leu813Ile
XM_011531978.1:c.2437C>A	XP_011530280.1:p.Leu813Ile
NM_001354819.1:c.2074C>A	NP_001341748.1:p.Leu692Ile
NR_148974.1:n.2378-32266C>A
XM_011531978.2:c.2437C>A	XP_011530280.1:p.Leu813Ile
NM_000901.5:c.2425C>A MANE Select	NP_000892.2:p.Leu809Ile
NM_001166104.2:c.2074C>A	NP_001159576.1:p.Leu692Ile
NR_148974.2:n.2272-32266C>A