Canonical Allele Identifier: CA2672314007

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148154505-CTTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154508_148154510del , CM000666.2:g.148154508_148154510del	GRCh38
NC_000004.11:g.149075659_149075661del , CM000666.1:g.149075659_149075661del	GRCh37
NC_000004.10:g.149295109_149295111del	NCBI36
NG_013350.1:g.293014_293016del

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2365+43_2365+45del MANE Select	ENSP00000350815.3:n.2365+43_2365+45del
ENST00000342437.8:c.2015-34220_2015-34218del	ENSP00000343907.4:n.2015-34220_2015-34218...
ENST00000344721.8:c.2365+43_2365+45del	ENSP00000341390.4:n.2365+43_2365+45del
ENST00000358102.7:c.2365+43_2365+45del	ENSP00000350815.3:n.2365+43_2365+45del
ENST00000503174.1:n.294+43_294+45del
ENST00000503313.1:n.562+43_562+45del
ENST00000511528.1:c.2377+43_2377+45del	ENSP00000421481.1:n.2377+43_2377+45del
ENST00000512865.5:c.2015-1895_2015-1893del	ENSP00000423510.1:n.2015-1895_2015-1893de...
ENST00000625323.2:c.2377+43_2377+45del	ENSP00000486719.1:n.2377+43_2377+45del
NM_000901.4:c.2365+43_2365+45del	NP_000892.2:n.2365+43_2365+45del
NM_001166104.1:c.2015-1895_2015-1893del	NP_001159576.1:n.2015-1895_2015-1893del
XM_011531975.1:c.2377+43_2377+45del	XP_011530277.1:n.2377+43_2377+45del
XM_011531976.1:c.2377+43_2377+45del	XP_011530278.1:n.2377+43_2377+45del
XM_011531977.1:c.2377+43_2377+45del	XP_011530279.1:n.2377+43_2377+45del
XM_011531978.1:c.2377+43_2377+45del	XP_011530280.1:n.2377+43_2377+45del
NM_001354819.1:c.2015-1895_2015-1893del	NP_001341748.1:n.2015-1895_2015-1893del
NR_148974.1:n.2378-34220_2378-34218del
XM_011531978.2:c.2377+43_2377+45del	XP_011530280.1:n.2377+43_2377+45del
NM_000901.5:c.2365+43_2365+45del MANE Select	NP_000892.2:n.2365+43_2365+45del
NM_001166104.2:c.2015-1895_2015-1893del	NP_001159576.1:n.2015-1895_2015-1893del
NR_148974.2:n.2272-34220_2272-34218del