Canonical Allele Identifier: CA2580591114

Gene: NR3C1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143403956A= , CM000667.2:g.143403956A=	GRCh38
NC_000005.9:g.142783521A= , CM000667.1:g.142783521A=	GRCh37
NC_000005.8:g.142763714A=	NCBI36
NG_009062.1:g.36557T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001018074.1:c.-13-3104T=	NP_001018084.1:n.-13-3104T=
NM_001018075.1:c.-13-3104T=	NP_001018085.1:n.-13-3104T=
NM_001018076.1:c.-14+420T=	NP_001018086.1:n.-14+420T=
NM_001018076.2:c.-14+420T=	NP_001018086.1:n.-14+420T=
NM_001018077.1:c.-13-3104T=	NP_001018087.1:n.-13-3104T=
NM_001364180.1:c.-14+1194T=	NP_001351109.1:n.-14+1194T=
NM_001364180.2:c.-14+1194T=	NP_001351109.1:n.-14+1194T=
NM_001364181.1:c.-14+30T=	NP_001351110.1:n.-14+30T=
NM_001364181.2:c.-14+30T=	NP_001351110.1:n.-14+30T=
NM_001364183.1:c.-13-3104T=	NP_001351112.1:n.-13-3104T=
NM_001364183.2:c.-13-3104T=	NP_001351112.1:n.-13-3104T=
NM_001364184.1:c.-14+420T=	NP_001351113.1:n.-14+420T=
NM_001364184.2:c.-14+420T=	NP_001351113.1:n.-14+420T=
NR_157096.1:n.107+420T=
NR_157096.2:n.107+420T=
ENST00000343796.6:c.-13-3104T=	ENSP00000343205.2:n.-13-3104T=
ENST00000394466.6:c.-14+30T=	ENSP00000377979.2:n.-14+30T=
ENST00000502892.5:c.-14+663T=	ENSP00000420856.1:n.-14+663T=
ENST00000503201.1:c.-14+420T=	ENSP00000427672.1:n.-14+420T=
ENST00000504572.5:c.-13-3104T=	ENSP00000422518.1:n.-13-3104T=
ENST00000514699.1:c.-14+1194T=	ENSP00000426478.1:n.-14+1194T=
XM_005268419.2:c.-14+420T=	XP_005268476.1:n.-14+420T=
XM_005268419.4:c.-14+420T=	XP_005268476.1:n.-14+420T=
XM_005268422.2:c.-13-3104T=	XP_005268479.1:n.-13-3104T=
XM_005268422.3:c.-13-3104T=	XP_005268479.1:n.-13-3104T=
XM_005268423.2:c.-14+30T=	XP_005268480.1:n.-14+30T=
XM_005268423.3:c.-14+30T=	XP_005268480.1:n.-14+30T=
XM_017009397.1:c.-14+30T=	XP_016864886.1:n.-14+30T=