Canonical Allele Identifier: CA1502460268

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148436700_148436709delinsGCACCGGAAA , CM000666.2:g.148436700_148436709delinsGCACCGGAAA	GRCh38
NC_000004.11:g.149357852_149357861delinsGCACCGGAAA , CM000666.1:g.149357852_149357861delinsGCACCGGAAA	GRCh37
NC_000004.10:g.149577302_149577311delinsGCACCGGAAA	NCBI36
NG_013350.1:g.10812_10821delinsTTTCCGGTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.152_161delinsTTTCCGGTGC MANE Select	ENSP00000350815.3:p.Val51=
ENST00000342437.8:c.152_161delinsTTTCCGGTGC	ENSP00000343907.4:p.Val51=
ENST00000344721.8:c.152_161delinsTTTCCGGTGC	ENSP00000341390.4:p.Val51=
ENST00000358102.7:c.152_161delinsTTTCCGGTGC	ENSP00000350815.3:p.Val51=
ENST00000511528.1:c.152_161delinsTTTCCGGTGC	ENSP00000421481.1:p.Val51=
ENST00000512865.5:c.152_161delinsTTTCCGGTGC	ENSP00000423510.1:p.Val51=
ENST00000625323.2:c.152_161delinsTTTCCGGTGC	ENSP00000486719.1:p.Val51=
NM_000901.4:c.152_161delinsTTTCCGGTGC	NP_000892.2:p.Val51=
NM_001166104.1:c.152_161delinsTTTCCGGTGC	NP_001159576.1:p.Val51=
XM_011531975.1:c.152_161delinsTTTCCGGTGC	XP_011530277.1:p.Val51=
XM_011531976.1:c.152_161delinsTTTCCGGTGC	XP_011530278.1:p.Val51=
XM_011531977.1:c.152_161delinsTTTCCGGTGC	XP_011530279.1:p.Val51=
XM_011531978.1:c.152_161delinsTTTCCGGTGC	XP_011530280.1:p.Val51=
NM_001354819.1:c.152_161delinsTTTCCGGTGC	NP_001341748.1:p.Val51=
NR_148974.1:n.515_524delinsTTTCCGGTGC
XM_011531978.2:c.152_161delinsTTTCCGGTGC	XP_011530280.1:p.Val51=
NM_000901.5:c.152_161delinsTTTCCGGTGC MANE Select	NP_000892.2:p.Val51=
NM_001166104.2:c.152_161delinsTTTCCGGTGC	NP_001159576.1:p.Val51=
NR_148974.2:n.409_418delinsTTTCCGGTGC