Canonical Allele Identifier: CA361870524

Gene: NR3C1

Linked Data

• MyVariant Identifiers: chr5:g.142689704A>G (hg19) ; chr5:g.143310139A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143310139A>G , CM000667.2:g.143310139A>G	GRCh38
NC_000005.9:g.142689704A>G , CM000667.1:g.142689704A>G	GRCh37
NC_000005.8:g.142669897A>G	NCBI36
NG_009062.1:g.130374T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394464.7:c.1426T>C MANE Select	ENSP00000377977.2:p.Cys476Arg
ENST00000652686.1:c.1426T>C	ENSP00000498663.1:p.Cys476Arg
ENST00000231509.7:c.1429T>C	ENSP00000231509.3:p.Cys477Arg
ENST00000343796.6:c.1426T>C	ENSP00000343205.2:p.Cys476Arg
ENST00000394464.6:c.1426T>C	ENSP00000377977.2:p.Cys476Arg
ENST00000394466.6:c.1429T>C	ENSP00000377979.2:p.Cys477Arg
ENST00000415690.6:c.1426T>C	ENSP00000387672.2:p.Cys476Arg
ENST00000424646.6:c.1348T>C	ENSP00000405282.2:p.Cys450Arg
ENST00000503201.1:c.1426T>C	ENSP00000427672.1:p.Cys476Arg
ENST00000504336.1:n.366T>C
ENST00000504572.5:c.1429T>C	ENSP00000422518.1:p.Cys477Arg
NM_000176.2:c.1426T>C	NP_000167.1:p.Cys476Arg
NM_001018074.1:c.1426T>C	NP_001018084.1:p.Cys476Arg
NM_001018075.1:c.1426T>C	NP_001018085.1:p.Cys476Arg
NM_001018076.1:c.1426T>C	NP_001018086.1:p.Cys476Arg
NM_001018077.1:c.1426T>C	NP_001018087.1:p.Cys476Arg
NM_001020825.1:c.1426T>C	NP_001018661.1:p.Cys476Arg
NM_001024094.1:c.1429T>C	NP_001019265.1:p.Cys477Arg
NM_001204258.1:c.1348T>C	NP_001191187.1:p.Cys450Arg
NM_001204259.1:c.1171T>C	NP_001191188.1:p.Cys391Arg
NM_001204260.1:c.1159T>C	NP_001191189.1:p.Cys387Arg
NM_001204261.1:c.1135T>C	NP_001191190.1:p.Cys379Arg
NM_001204262.1:c.481T>C	NP_001191191.1:p.Cys161Arg
NM_001204263.1:c.436T>C	NP_001191192.1:p.Cys146Arg
NM_001204264.1:c.421T>C	NP_001191193.1:p.Cys141Arg
NM_001204265.1:c.1426T>C	NP_001191194.1:p.Cys476Arg
XM_005268419.2:c.1429T>C	XP_005268476.1:p.Cys477Arg
XM_005268420.3:c.1429T>C	XP_005268477.1:p.Cys477Arg
XM_005268422.2:c.1429T>C	XP_005268479.1:p.Cys477Arg
XM_005268423.2:c.1429T>C	XP_005268480.1:p.Cys477Arg
XM_011537637.1:c.235T>C	XP_011535939.1:p.Cys79Arg
NR_157096.1:n.349T>C
XM_005268419.4:c.1429T>C	XP_005268476.1:p.Cys477Arg
XM_005268420.4:c.1429T>C	XP_005268477.1:p.Cys477Arg
XM_005268422.3:c.1429T>C	XP_005268479.1:p.Cys477Arg
XM_005268423.3:c.1429T>C	XP_005268480.1:p.Cys477Arg
XM_011537637.3:c.235T>C	XP_011535939.1:p.Cys79Arg
XM_017009397.1:c.1426T>C	XP_016864886.1:p.Cys476Arg
XM_017009398.1:c.1426T>C	XP_016864887.1:p.Cys476Arg
NM_000176.3:c.1426T>C MANE Select	NP_000167.1:p.Cys476Arg
NM_001364180.1:c.1426T>C	NP_001351109.1:p.Cys476Arg
NM_001364181.1:c.1426T>C	NP_001351110.1:p.Cys476Arg
NM_001364182.1:c.1426T>C	NP_001351111.1:p.Cys476Arg
NM_001364183.1:c.1429T>C	NP_001351112.1:p.Cys477Arg
NM_001364184.1:c.1429T>C	NP_001351113.1:p.Cys477Arg
NM_001364185.1:c.1429T>C	NP_001351114.1:p.Cys477Arg
NM_001018076.2:c.1426T>C	NP_001018086.1:p.Cys476Arg
NM_001020825.2:c.1426T>C	NP_001018661.1:p.Cys476Arg
NM_001024094.2:c.1429T>C	NP_001019265.1:p.Cys477Arg
NM_001204258.2:c.1348T>C	NP_001191187.1:p.Cys450Arg
NM_001204259.2:c.1171T>C	NP_001191188.1:p.Cys391Arg
NM_001204260.2:c.1159T>C	NP_001191189.1:p.Cys387Arg
NM_001204261.2:c.1135T>C	NP_001191190.1:p.Cys379Arg
NM_001204262.2:c.481T>C	NP_001191191.1:p.Cys161Arg
NM_001204263.2:c.436T>C	NP_001191192.1:p.Cys146Arg
NM_001204264.2:c.421T>C	NP_001191193.1:p.Cys141Arg
NM_001204265.2:c.1426T>C	NP_001191194.1:p.Cys476Arg
NM_001364180.2:c.1426T>C	NP_001351109.1:p.Cys476Arg
NM_001364181.2:c.1426T>C	NP_001351110.1:p.Cys476Arg
NM_001364183.2:c.1429T>C	NP_001351112.1:p.Cys477Arg
NM_001364184.2:c.1429T>C	NP_001351113.1:p.Cys477Arg
NR_157096.2:n.349T>C