Canonical Allele Identifier: CA2763954972

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152640_148152641insCCC , CM000666.2:g.148152640_148152641insCCC	GRCh38
NC_000004.11:g.149073791_149073792insCCC , CM000666.1:g.149073791_149073792insCCC	GRCh37
NC_000004.10:g.149293241_149293242insCCC	NCBI36
NG_013350.1:g.294881_294882insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2366-28_2366-27insGGG MANE Select	ENSP00000350815.3:n.2366-28_2366-27insGGG
ENST00000342437.8:c.2015-32353_2015-32352insGGG	ENSP00000343907.4:n.2015-32353_2015-32352insGGG
ENST00000344721.8:c.2366-28_2366-27insGGG	ENSP00000341390.4:n.2366-28_2366-27insGGG
ENST00000358102.7:c.2366-28_2366-27insGGG	ENSP00000350815.3:n.2366-28_2366-27insGGG
ENST00000503174.1:n.295-28_295-27insGGG
ENST00000503313.1:n.563-28_563-27insGGG
ENST00000511528.1:c.2378-28_2378-27insGGG	ENSP00000421481.1:n.2378-28_2378-27insGGG
ENST00000512865.5:c.2015-28_2015-27insGGG	ENSP00000423510.1:n.2015-28_2015-27insGGG
ENST00000625323.2:c.2378-28_2378-27insGGG	ENSP00000486719.1:n.2378-28_2378-27insGGG
NM_000901.4:c.2366-28_2366-27insGGG	NP_000892.2:n.2366-28_2366-27insGGG
NM_001166104.1:c.2015-28_2015-27insGGG	NP_001159576.1:n.2015-28_2015-27insGGG
XM_011531975.1:c.2378-28_2378-27insGGG	XP_011530277.1:n.2378-28_2378-27insGGG
XM_011531976.1:c.2378-28_2378-27insGGG	XP_011530278.1:n.2378-28_2378-27insGGG
XM_011531977.1:c.2378-28_2378-27insGGG	XP_011530279.1:n.2378-28_2378-27insGGG
XM_011531978.1:c.2378-28_2378-27insGGG	XP_011530280.1:n.2378-28_2378-27insGGG
NM_001354819.1:c.2015-28_2015-27insGGG	NP_001341748.1:n.2015-28_2015-27insGGG
NR_148974.1:n.2378-32353_2378-32352insGGG
XM_011531978.2:c.2378-28_2378-27insGGG	XP_011530280.1:n.2378-28_2378-27insGGG
NM_000901.5:c.2366-28_2366-27insGGG MANE Select	NP_000892.2:n.2366-28_2366-27insGGG
NM_001166104.2:c.2015-28_2015-27insGGG	NP_001159576.1:n.2015-28_2015-27insGGG
NR_148974.2:n.2272-32353_2272-32352insGGG