Canonical Allele Identifier: CA2521045012

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148299961_148299991dup , CM000666.2:g.148299961_148299991dup	GRCh38
NC_000004.11:g.149221113_149221143dup , CM000666.1:g.149221113_149221143dup	GRCh37
NC_000004.10:g.149440563_149440593dup	NCBI36
NG_013350.1:g.147530_147560dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.1758-39874_1758-39844dup MANE Select	ENSP00000350815.3:n.1758-39874_1758-39844dup
ENST00000342437.8:c.1758-39874_1758-39844dup	ENSP00000343907.4:n.1758-39874_1758-39844dup
ENST00000344721.8:c.1758-39874_1758-39844dup	ENSP00000341390.4:n.1758-39874_1758-39844dup
ENST00000358102.7:c.1758-39874_1758-39844dup	ENSP00000350815.3:n.1758-39874_1758-39844dup
ENST00000504753.1:n.207-39874_207-39844dup
ENST00000511528.1:c.1758-39874_1758-39844dup	ENSP00000421481.1:n.1758-39874_1758-39844dup
ENST00000512865.5:c.1758-39874_1758-39844dup	ENSP00000423510.1:n.1758-39874_1758-39844dup
ENST00000625323.2:c.1758-39874_1758-39844dup	ENSP00000486719.1:n.1758-39874_1758-39844dup
NM_000901.4:c.1758-39874_1758-39844dup	NP_000892.2:n.1758-39874_1758-39844dup
NM_001166104.1:c.1758-39874_1758-39844dup	NP_001159576.1:n.1758-39874_1758-39844dup
XM_011531975.1:c.1758-39874_1758-39844dup	XP_011530277.1:n.1758-39874_1758-39844dup
XM_011531976.1:c.1758-39874_1758-39844dup	XP_011530278.1:n.1758-39874_1758-39844dup
XM_011531977.1:c.1758-39874_1758-39844dup	XP_011530279.1:n.1758-39874_1758-39844dup
XM_011531978.1:c.1758-39874_1758-39844dup	XP_011530280.1:n.1758-39874_1758-39844dup
NM_001354819.1:c.1758-39874_1758-39844dup	NP_001341748.1:n.1758-39874_1758-39844dup
NR_148974.1:n.2121-39874_2121-39844dup
XM_011531978.2:c.1758-39874_1758-39844dup	XP_011530280.1:n.1758-39874_1758-39844dup
NM_000901.5:c.1758-39874_1758-39844dup MANE Select	NP_000892.2:n.1758-39874_1758-39844dup
NM_001166104.2:c.1758-39874_1758-39844dup	NP_001159576.1:n.1758-39874_1758-39844dup
NR_148974.2:n.2015-39874_2015-39844dup