Canonical Allele Identifier: CA2516201557

Gene: NR3C1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143426284_143426285insTC , CM000667.2:g.143426284_143426285insTC	GRCh38
NC_000005.9:g.142805849_142805850insTC , CM000667.1:g.142805849_142805850insTC	GRCh37
NC_000005.8:g.142786042_142786043insTC	NCBI36
NG_009062.1:g.14228_14229insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+8247_-14+8248insGA	ENSP00000343205.2:n.-14+8247_-14+8248insGA
ENST00000503701.1:n.352+7434_352+7435insGA
ENST00000504572.5:c.-14+7434_-14+7435insGA	ENSP00000422518.1:n.-14+7434_-14+7435insGA
ENST00000505058.5:n.241+8247_241+8248insGA
NM_001018074.1:c.-14+8919_-14+8920insGA	NP_001018084.1:n.-14+8919_-14+8920insGA
NM_001018075.1:c.-14+9016_-14+9017insGA	NP_001018085.1:n.-14+9016_-14+9017insGA
NM_001018077.1:c.-14+8247_-14+8248insGA	NP_001018087.1:n.-14+8247_-14+8248insGA
XM_005268422.2:c.-14+8247_-14+8248insGA	XP_005268479.1:n.-14+8247_-14+8248insGA
XM_005268422.3:c.-14+8247_-14+8248insGA	XP_005268479.1:n.-14+8247_-14+8248insGA
NM_001364183.1:c.-14+7434_-14+7435insGA	NP_001351112.1:n.-14+7434_-14+7435insGA
NM_001364183.2:c.-14+7434_-14+7435insGA	NP_001351112.1:n.-14+7434_-14+7435insGA