Canonical Allele Identifier: CA788817327

Gene: NR3C2

Linked Data

• dbSNP Id: rs1221524531
• gnomAD v3: 4-148081261-TTAAAAACAGG-T
• gnomAD v4: 4-148081261-TTAAAAACAGG-T
• MyVariant Identifiers: chr4:g.149002413_149002422del (hg19) ; chr4:g.148081262_148081271del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081263_148081272del , CM000666.2:g.148081263_148081272del	GRCh38
NC_000004.11:g.149002414_149002423del , CM000666.1:g.149002414_149002423del	GRCh37
NC_000004.10:g.149221864_149221873del	NCBI36
NG_013350.1:g.366251_366260del

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.*73_*82del MANE Select	ENSP00000350815.3:n.*73_*82del
ENST00000342437.8:c.*411_*420del	ENSP00000343907.4:n.*411_*420del
ENST00000344721.8:c.*73_*82del	ENSP00000341390.4:n.*73_*82del
ENST00000358102.7:c.*73_*82del	ENSP00000350815.3:n.*73_*82del
ENST00000512865.5:c.*73_*82del	ENSP00000423510.1:n.*73_*82del
ENST00000625323.2:c.*73_*82del	ENSP00000486719.1:n.*73_*82del
NM_000901.4:c.*73_*82del	NP_000892.2:n.*73_*82del
NM_001166104.1:c.*73_*82del	NP_001159576.1:n.*73_*82del
XM_011531975.1:c.*73_*82del	XP_011530277.1:n.*73_*82del
XM_011531976.1:c.*73_*82del	XP_011530278.1:n.*73_*82del
XM_011531977.1:c.*73_*82del	XP_011530279.1:n.*73_*82del
NM_001354819.1:c.*73_*82del	NP_001341748.1:n.*73_*82del
NR_148974.1:n.2895_2904del
NM_000901.5:c.*73_*82del MANE Select	NP_000892.2:n.*73_*82del
NM_001166104.2:c.*73_*82del	NP_001159576.1:n.*73_*82del
NR_148974.2:n.2789_2798del