Canonical Allele Identifier: CA2672314006

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148154503-GACT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154504_148154506del , CM000666.2:g.148154504_148154506del	GRCh38
NC_000004.11:g.149075655_149075657del , CM000666.1:g.149075655_149075657del	GRCh37
NC_000004.10:g.149295105_149295107del	NCBI36
NG_013350.1:g.293016_293018del

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2365+45_2365+47del MANE Select	ENSP00000350815.3:n.2365+45_2365+47del
ENST00000342437.8:c.2015-34218_2015-34216del	ENSP00000343907.4:n.2015-34218_2015-34216...
ENST00000344721.8:c.2365+45_2365+47del	ENSP00000341390.4:n.2365+45_2365+47del
ENST00000358102.7:c.2365+45_2365+47del	ENSP00000350815.3:n.2365+45_2365+47del
ENST00000503174.1:n.294+45_294+47del
ENST00000503313.1:n.562+45_562+47del
ENST00000511528.1:c.2377+45_2377+47del	ENSP00000421481.1:n.2377+45_2377+47del
ENST00000512865.5:c.2015-1893_2015-1891del	ENSP00000423510.1:n.2015-1893_2015-1891de...
ENST00000625323.2:c.2377+45_2377+47del	ENSP00000486719.1:n.2377+45_2377+47del
NM_000901.4:c.2365+45_2365+47del	NP_000892.2:n.2365+45_2365+47del
NM_001166104.1:c.2015-1893_2015-1891del	NP_001159576.1:n.2015-1893_2015-1891del
XM_011531975.1:c.2377+45_2377+47del	XP_011530277.1:n.2377+45_2377+47del
XM_011531976.1:c.2377+45_2377+47del	XP_011530278.1:n.2377+45_2377+47del
XM_011531977.1:c.2377+45_2377+47del	XP_011530279.1:n.2377+45_2377+47del
XM_011531978.1:c.2377+45_2377+47del	XP_011530280.1:n.2377+45_2377+47del
NM_001354819.1:c.2015-1893_2015-1891del	NP_001341748.1:n.2015-1893_2015-1891del
NR_148974.1:n.2378-34218_2378-34216del
XM_011531978.2:c.2377+45_2377+47del	XP_011530280.1:n.2377+45_2377+47del
NM_000901.5:c.2365+45_2365+47del MANE Select	NP_000892.2:n.2365+45_2365+47del
NM_001166104.2:c.2015-1893_2015-1891del	NP_001159576.1:n.2015-1893_2015-1891del
NR_148974.2:n.2272-34218_2272-34216del