Canonical Allele Identifier: CA2672314351

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148195009-AGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148195016_148195018del , CM000666.2:g.148195016_148195018del	GRCh38
NC_000004.11:g.149116167_149116169del , CM000666.1:g.149116167_149116169del	GRCh37
NC_000004.10:g.149335617_149335619del	NCBI36
NG_013350.1:g.252510_252512del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.1898-150_1898-148del MANE Select	ENSP00000350815.3:n.1898-150_1898-148del
ENST00000342437.8:c.1898-150_1898-148del	ENSP00000343907.4:n.1898-150_1898-148del
ENST00000344721.8:c.1898-150_1898-148del	ENSP00000341390.4:n.1898-150_1898-148del
ENST00000358102.7:c.1898-150_1898-148del	ENSP00000350815.3:n.1898-150_1898-148del
ENST00000503313.1:n.95-150_95-148del
ENST00000504753.1:n.347-150_347-148del
ENST00000511528.1:c.1910-150_1910-148del	ENSP00000421481.1:n.1910-150_1910-148del
ENST00000512865.5:c.1898-150_1898-148del	ENSP00000423510.1:n.1898-150_1898-148del
ENST00000625323.2:c.1910-150_1910-148del	ENSP00000486719.1:n.1910-150_1910-148del
NM_000901.4:c.1898-150_1898-148del	NP_000892.2:n.1898-150_1898-148del
NM_001166104.1:c.1898-150_1898-148del	NP_001159576.1:n.1898-150_1898-148del
XM_011531975.1:c.1910-150_1910-148del	XP_011530277.1:n.1910-150_1910-148del
XM_011531976.1:c.1910-150_1910-148del	XP_011530278.1:n.1910-150_1910-148del
XM_011531977.1:c.1910-150_1910-148del	XP_011530279.1:n.1910-150_1910-148del
XM_011531978.1:c.1910-150_1910-148del	XP_011530280.1:n.1910-150_1910-148del
NM_001354819.1:c.1898-150_1898-148del	NP_001341748.1:n.1898-150_1898-148del
NR_148974.1:n.2261-150_2261-148del
XM_011531978.2:c.1910-150_1910-148del	XP_011530280.1:n.1910-150_1910-148del
NM_000901.5:c.1898-150_1898-148del MANE Select	NP_000892.2:n.1898-150_1898-148del
NM_001166104.2:c.1898-150_1898-148del	NP_001159576.1:n.1898-150_1898-148del
NR_148974.2:n.2155-150_2155-148del