Canonical Allele Identifier: CA1502470355

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148442502_148442505delinsCTGG , CM000666.2:g.148442502_148442505delinsCTGG	GRCh38
NC_000004.11:g.149363654_149363657delinsCTGG , CM000666.1:g.149363654_149363657delinsCTGG	GRCh37
NC_000004.10:g.149583104_149583107delinsCTGG	NCBI36
NG_013350.1:g.5016_5019delinsCCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344721.8:c.-3+2021_-3+2024delinsCCAG	ENSP00000341390.4:n.-3+2021_-3+2024delinsCCAG
ENST00000358102.7:c.-348_-345delinsCCAG	ENSP00000350815.3:n.-348_-345delinsCCAG
ENST00000625323.2:c.-348_-345delinsCCAG	ENSP00000486719.1:n.-348_-345delinsCCAG
NM_000901.4:c.-348_-345delinsCCAG	NP_000892.2:n.-348_-345delinsCCAG
NM_001166104.1:c.-348_-345delinsCCAG	NP_001159576.1:n.-348_-345delinsCCAG
XM_011531975.1:c.-348_-345delinsCCAG	XP_011530277.1:n.-348_-345delinsCCAG
XM_011531976.1:c.-3+2021_-3+2024delinsCCAG	XP_011530278.1:n.-3+2021_-3+2024delinsCCAG
XM_011531977.1:c.-3+2695_-3+2698delinsCCAG	XP_011530279.1:n.-3+2695_-3+2698delinsCCAG
XM_011531978.1:c.-348_-345delinsCCAG	XP_011530280.1:n.-348_-345delinsCCAG
NM_001354819.1:c.-3+2021_-3+2024delinsCCAG	NP_001341748.1:n.-3+2021_-3+2024delinsCCAG
NR_148974.1:n.16_19delinsCCAG
XM_011531978.2:c.-348_-345delinsCCAG	XP_011530280.1:n.-348_-345delinsCCAG