Canonical Allele Identifier: CA441754201

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149073602_149073605del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152455_148152458del , CM000666.2:g.148152455_148152458del	GRCh38
NC_000004.11:g.149073606_149073609del , CM000666.1:g.149073606_149073609del	GRCh37
NC_000004.10:g.149293056_149293059del	NCBI36
NG_013350.1:g.295068_295071del

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2510+15_2510+18del MANE Select	ENSP00000350815.3:n.2510+15_2510+18del
ENST00000342437.8:c.2015-32166_2015-32163del	ENSP00000343907.4:n.2015-32166_2015-32163...
ENST00000344721.8:c.2510+15_2510+18del	ENSP00000341390.4:n.2510+15_2510+18del
ENST00000358102.7:c.2510+15_2510+18del	ENSP00000350815.3:n.2510+15_2510+18del
ENST00000503174.1:n.454_457del
ENST00000503313.1:n.707+15_707+18del
ENST00000511528.1:c.2522+15_2522+18del	ENSP00000421481.1:n.2522+15_2522+18del
ENST00000512865.5:c.2159+15_2159+18del	ENSP00000423510.1:n.2159+15_2159+18del
ENST00000625323.2:c.2522+15_2522+18del	ENSP00000486719.1:n.2522+15_2522+18del
NM_000901.4:c.2510+15_2510+18del	NP_000892.2:n.2510+15_2510+18del
NM_001166104.1:c.2159+15_2159+18del	NP_001159576.1:n.2159+15_2159+18del
XM_011531975.1:c.2522+15_2522+18del	XP_011530277.1:n.2522+15_2522+18del
XM_011531976.1:c.2522+15_2522+18del	XP_011530278.1:n.2522+15_2522+18del
XM_011531977.1:c.2522+15_2522+18del	XP_011530279.1:n.2522+15_2522+18del
XM_011531978.1:c.2522+15_2522+18del	XP_011530280.1:n.2522+15_2522+18del
NM_001354819.1:c.2159+15_2159+18del	NP_001341748.1:n.2159+15_2159+18del
NR_148974.1:n.2378-32166_2378-32163del
XM_011531978.2:c.2522+15_2522+18del	XP_011530280.1:n.2522+15_2522+18del
NM_000901.5:c.2510+15_2510+18del MANE Select	NP_000892.2:n.2510+15_2510+18del
NM_001166104.2:c.2159+15_2159+18del	NP_001159576.1:n.2159+15_2159+18del
NR_148974.2:n.2272-32166_2272-32163del