Canonical Allele Identifier: CA1082411663

Gene: NR3C1

Linked Data

• dbSNP Id: rs1751526998
• gnomAD v3: 5-143426317-AAATT-A
• gnomAD v4: 5-143426317-AAATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143426320_143426323del , CM000667.2:g.143426320_143426323del	GRCh38
NC_000005.9:g.142805885_142805888del , CM000667.1:g.142805885_142805888del	GRCh37
NC_000005.8:g.142786078_142786081del	NCBI36
NG_009062.1:g.14192_14195del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+8211_-14+8214del	ENSP00000343205.2:n.-14+8211_-14+8214del
ENST00000503701.1:n.352+7398_352+7401del
ENST00000504572.5:c.-14+7398_-14+7401del	ENSP00000422518.1:n.-14+7398_-14+7401del
ENST00000505058.5:n.241+8211_241+8214del
NM_001018074.1:c.-14+8883_-14+8886del	NP_001018084.1:n.-14+8883_-14+8886del
NM_001018075.1:c.-14+8980_-14+8983del	NP_001018085.1:n.-14+8980_-14+8983del
NM_001018077.1:c.-14+8211_-14+8214del	NP_001018087.1:n.-14+8211_-14+8214del
XM_005268422.2:c.-14+8211_-14+8214del	XP_005268479.1:n.-14+8211_-14+8214del
XM_005268422.3:c.-14+8211_-14+8214del	XP_005268479.1:n.-14+8211_-14+8214del
NM_001364183.1:c.-14+7398_-14+7401del	NP_001351112.1:n.-14+7398_-14+7401del
NM_001364183.2:c.-14+7398_-14+7401del	NP_001351112.1:n.-14+7398_-14+7401del