Canonical Allele Identifier: CA2672313823

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148152388-ATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152390_148152391del , CM000666.2:g.148152390_148152391del	GRCh38
NC_000004.11:g.149073541_149073542del , CM000666.1:g.149073541_149073542del	GRCh37
NC_000004.10:g.149292991_149292992del	NCBI36
NG_013350.1:g.295132_295133del

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2510+79_2510+80del MANE Select	ENSP00000350815.3:n.2510+79_2510+80del
ENST00000342437.8:c.2015-32102_2015-32101del	ENSP00000343907.4:n.2015-32102_2015-32101...
ENST00000344721.8:c.2510+79_2510+80del	ENSP00000341390.4:n.2510+79_2510+80del
ENST00000358102.7:c.2510+79_2510+80del	ENSP00000350815.3:n.2510+79_2510+80del
ENST00000503313.1:n.707+79_707+80del
ENST00000511528.1:c.2522+79_2522+80del	ENSP00000421481.1:n.2522+79_2522+80del
ENST00000512865.5:c.2159+79_2159+80del	ENSP00000423510.1:n.2159+79_2159+80del
ENST00000625323.2:c.2522+79_2522+80del	ENSP00000486719.1:n.2522+79_2522+80del
NM_000901.4:c.2510+79_2510+80del	NP_000892.2:n.2510+79_2510+80del
NM_001166104.1:c.2159+79_2159+80del	NP_001159576.1:n.2159+79_2159+80del
XM_011531975.1:c.2522+79_2522+80del	XP_011530277.1:n.2522+79_2522+80del
XM_011531976.1:c.2522+79_2522+80del	XP_011530278.1:n.2522+79_2522+80del
XM_011531977.1:c.2522+79_2522+80del	XP_011530279.1:n.2522+79_2522+80del
XM_011531978.1:c.2522+79_2522+80del	XP_011530280.1:n.2522+79_2522+80del
NM_001354819.1:c.2159+79_2159+80del	NP_001341748.1:n.2159+79_2159+80del
NR_148974.1:n.2378-32102_2378-32101del
XM_011531978.2:c.2522+79_2522+80del	XP_011530280.1:n.2522+79_2522+80del
NM_000901.5:c.2510+79_2510+80del MANE Select	NP_000892.2:n.2510+79_2510+80del
NM_001166104.2:c.2159+79_2159+80del	NP_001159576.1:n.2159+79_2159+80del
NR_148974.2:n.2272-32102_2272-32101del