Canonical Allele Identifier: CA1502470190

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148442461_148442463delinsGGA , CM000666.2:g.148442461_148442463delinsGGA	GRCh38
NC_000004.11:g.149363613_149363615delinsGGA , CM000666.1:g.149363613_149363615delinsGGA	GRCh37
NC_000004.10:g.149583063_149583065delinsGGA	NCBI36
NG_013350.1:g.5058_5060delinsTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344721.8:c.-3+2063_-3+2065delinsTCC	ENSP00000341390.4:n.-3+2063_-3+2065delinsTCC
ENST00000358102.7:c.-306_-304delinsTCC	ENSP00000350815.3:n.-306_-304delinsTCC
ENST00000625323.2:c.-306_-304delinsTCC	ENSP00000486719.1:n.-306_-304delinsTCC
NM_000901.4:c.-306_-304delinsTCC	NP_000892.2:n.-306_-304delinsTCC
NM_001166104.1:c.-306_-304delinsTCC	NP_001159576.1:n.-306_-304delinsTCC
XM_011531975.1:c.-306_-304delinsTCC	XP_011530277.1:n.-306_-304delinsTCC
XM_011531976.1:c.-3+2063_-3+2065delinsTCC	XP_011530278.1:n.-3+2063_-3+2065delinsTCC
XM_011531977.1:c.-3+2737_-3+2739delinsTCC	XP_011530279.1:n.-3+2737_-3+2739delinsTCC
XM_011531978.1:c.-306_-304delinsTCC	XP_011530280.1:n.-306_-304delinsTCC
NM_001354819.1:c.-3+2063_-3+2065delinsTCC	NP_001341748.1:n.-3+2063_-3+2065delinsTCC
NR_148974.1:n.58_60delinsTCC
XM_011531978.2:c.-306_-304delinsTCC	XP_011530280.1:n.-306_-304delinsTCC