Canonical Allele Identifier: CA645539847

Gene: NR3C2

Linked Data

• COSMIC: COSM1695060

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154805_148154806delinsAA , CM000666.2:g.148154805_148154806delinsAA	GRCh38
NC_000004.11:g.149075956_149075957delinsAA , CM000666.1:g.149075956_149075957delinsAA	GRCh37
NC_000004.10:g.149295406_149295407delinsAA	NCBI36
NG_013350.1:g.292716_292717delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2110_2111delinsTT MANE Select	ENSP00000350815.3:p.Pro704Leu
ENST00000342437.8:c.2015-34518_2015-34517delinsTT	ENSP00000343907.4:n.2015-34518_2015-34517...
ENST00000344721.8:c.2110_2111delinsTT	ENSP00000341390.4:p.Pro704Leu
ENST00000358102.7:c.2110_2111delinsTT	ENSP00000350815.3:p.Pro704Leu
ENST00000503174.1:n.39_40delinsTT
ENST00000503313.1:n.307_308delinsTT
ENST00000511528.1:c.2122_2123delinsTT	ENSP00000421481.1:p.Pro708Leu
ENST00000512865.5:c.2015-2193_2015-2192delinsTT	ENSP00000423510.1:n.2015-2193_2015-2192de...
ENST00000625323.2:c.2122_2123delinsTT	ENSP00000486719.1:p.Pro708Leu
NM_000901.4:c.2110_2111delinsTT	NP_000892.2:p.Pro704Leu
NM_001166104.1:c.2015-2193_2015-2192delinsTT	NP_001159576.1:n.2015-2193_2015-2192delin...
XM_011531975.1:c.2122_2123delinsTT	XP_011530277.1:p.Pro708Leu
XM_011531976.1:c.2122_2123delinsTT	XP_011530278.1:p.Pro708Leu
XM_011531977.1:c.2122_2123delinsTT	XP_011530279.1:p.Pro708Leu
XM_011531978.1:c.2122_2123delinsTT	XP_011530280.1:p.Pro708Leu
NM_001354819.1:c.2015-2193_2015-2192delinsTT	NP_001341748.1:n.2015-2193_2015-2192delin...
NR_148974.1:n.2378-34518_2378-34517delinsTT
XM_011531978.2:c.2122_2123delinsTT	XP_011530280.1:p.Pro708Leu
NM_000901.5:c.2110_2111delinsTT MANE Select	NP_000892.2:p.Pro704Leu
NM_001166104.2:c.2015-2193_2015-2192delinsTT	NP_001159576.1:n.2015-2193_2015-2192delin...
NR_148974.2:n.2272-34518_2272-34517delinsTT