Canonical Allele Identifier: CA2672312839

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148081262-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081267dup , CM000666.2:g.148081267dup	GRCh38
NC_000004.11:g.149002418dup , CM000666.1:g.149002418dup	GRCh37
NC_000004.10:g.149221868dup	NCBI36
NG_013350.1:g.366259dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.*81dup MANE Select	ENSP00000350815.3:n.*81dup
ENST00000342437.8:c.*419dup	ENSP00000343907.4:n.*419dup
ENST00000344721.8:c.*81dup	ENSP00000341390.4:n.*81dup
ENST00000358102.7:c.*81dup	ENSP00000350815.3:n.*81dup
ENST00000512865.5:c.*81dup	ENSP00000423510.1:n.*81dup
ENST00000625323.2:c.*81dup	ENSP00000486719.1:n.*81dup
NM_000901.4:c.*81dup	NP_000892.2:n.*81dup
NM_001166104.1:c.*81dup	NP_001159576.1:n.*81dup
XM_011531975.1:c.*81dup	XP_011530277.1:n.*81dup
XM_011531976.1:c.*81dup	XP_011530278.1:n.*81dup
XM_011531977.1:c.*81dup	XP_011530279.1:n.*81dup
NM_001354819.1:c.*81dup	NP_001341748.1:n.*81dup
NR_148974.1:n.2903dup
NM_000901.5:c.*81dup MANE Select	NP_000892.2:n.*81dup
NM_001166104.2:c.*81dup	NP_001159576.1:n.*81dup
NR_148974.2:n.2797dup