Canonical Allele Identifier: CA2527733187
Gene: NR3C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148390505_148390506insCATTTGAATTC , CM000666.2:g.148390505_148390506insCATTTGAATTC GRCh38
NC_000004.11:g.149311657_149311658insCATTTGAATTC , CM000666.1:g.149311657_149311658insCATTTGAATTC GRCh37
NC_000004.10:g.149531107_149531108insCATTTGAATTC NCBI36
NG_013350.1:g.57015_57016insGAATTCAAATG

Transcript Alleles

HGVS Amino-acid change
ENST00000358102.8:c.1757+44598_1757+44599insGAATTCAAATG MANE Select ENSP00000350815.3:n.1757+44598_1757+44599...
ENST00000342437.8:c.1757+44598_1757+44599insGAATTCAAATG ENSP00000343907.4:n.1757+44598_1757+44599...
ENST00000344721.8:c.1757+44598_1757+44599insGAATTCAAATG ENSP00000341390.4:n.1757+44598_1757+44599...
ENST00000358102.7:c.1757+44598_1757+44599insGAATTCAAATG ENSP00000350815.3:n.1757+44598_1757+44599...
ENST00000511528.1:c.1757+44598_1757+44599insGAATTCAAATG ENSP00000421481.1:n.1757+44598_1757+44599...
ENST00000512865.5:c.1757+44598_1757+44599insGAATTCAAATG ENSP00000423510.1:n.1757+44598_1757+44599...
ENST00000625323.2:c.1757+44598_1757+44599insGAATTCAAATG ENSP00000486719.1:n.1757+44598_1757+44599...
NM_000901.4:c.1757+44598_1757+44599insGAATTCAAATG NP_000892.2:n.1757+44598_1757+44599insGAA...
NM_001166104.1:c.1757+44598_1757+44599insGAATTCAAATG NP_001159576.1:n.1757+44598_1757+44599ins...
XM_011531975.1:c.1757+44598_1757+44599insGAATTCAAATG XP_011530277.1:n.1757+44598_1757+44599ins...
XM_011531976.1:c.1757+44598_1757+44599insGAATTCAAATG XP_011530278.1:n.1757+44598_1757+44599ins...
XM_011531977.1:c.1757+44598_1757+44599insGAATTCAAATG XP_011530279.1:n.1757+44598_1757+44599ins...
XM_011531978.1:c.1757+44598_1757+44599insGAATTCAAATG XP_011530280.1:n.1757+44598_1757+44599ins...
NM_001354819.1:c.1757+44598_1757+44599insGAATTCAAATG NP_001341748.1:n.1757+44598_1757+44599ins...
NR_148974.1:n.2120+44598_2120+44599insGAATTCAAATG
XM_011531978.2:c.1757+44598_1757+44599insGAATTCAAATG XP_011530280.1:n.1757+44598_1757+44599ins...
NM_000901.5:c.1757+44598_1757+44599insGAATTCAAATG MANE Select NP_000892.2:n.1757+44598_1757+44599insGAA...
NM_001166104.2:c.1757+44598_1757+44599insGAATTCAAATG NP_001159576.1:n.1757+44598_1757+44599ins...
NR_148974.2:n.2014+44598_2014+44599insGAATTCAAATG