Canonical Allele Identifier: CA2763962126

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148194961del , CM000666.2:g.148194961del	GRCh38
NC_000004.11:g.149116112del , CM000666.1:g.149116112del	GRCh37
NC_000004.10:g.149335562del	NCBI36
NG_013350.1:g.252561del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.1898-99del MANE Select	ENSP00000350815.3:n.1898-99del
ENST00000342437.8:c.1898-99del	ENSP00000343907.4:n.1898-99del
ENST00000344721.8:c.1898-99del	ENSP00000341390.4:n.1898-99del
ENST00000358102.7:c.1898-99del	ENSP00000350815.3:n.1898-99del
ENST00000503313.1:n.95-99del
ENST00000504753.1:n.347-99del
ENST00000511528.1:c.1910-99del	ENSP00000421481.1:n.1910-99del
ENST00000512865.5:c.1898-99del	ENSP00000423510.1:n.1898-99del
ENST00000625323.2:c.1910-99del	ENSP00000486719.1:n.1910-99del
NM_000901.4:c.1898-99del	NP_000892.2:n.1898-99del
NM_001166104.1:c.1898-99del	NP_001159576.1:n.1898-99del
XM_011531975.1:c.1910-99del	XP_011530277.1:n.1910-99del
XM_011531976.1:c.1910-99del	XP_011530278.1:n.1910-99del
XM_011531977.1:c.1910-99del	XP_011530279.1:n.1910-99del
XM_011531978.1:c.1910-99del	XP_011530280.1:n.1910-99del
NM_001354819.1:c.1898-99del	NP_001341748.1:n.1898-99del
NR_148974.1:n.2261-99del
XM_011531978.2:c.1910-99del	XP_011530280.1:n.1910-99del
NM_000901.5:c.1898-99del MANE Select	NP_000892.2:n.1898-99del
NM_001166104.2:c.1898-99del	NP_001159576.1:n.1898-99del
NR_148974.2:n.2155-99del