Canonical Allele Identifier: CA361868584

Gene: NR3C1

Linked Data

• MyVariant Identifiers: chr5:g.142661542A>G (hg19) ; chr5:g.143281977A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143281977A>G , CM000667.2:g.143281977A>G	GRCh38
NC_000005.9:g.142661542A>G , CM000667.1:g.142661542A>G	GRCh37
NC_000005.8:g.142641735A>G	NCBI36
NG_009062.1:g.158536T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394464.7:c.2246T>C MANE Select	ENSP00000377977.2:p.Phe749Ser
ENST00000652686.1:c.2153T>C	ENSP00000498663.1:p.Phe718Ser
ENST00000231509.7:c.2249T>C	ENSP00000231509.3:p.Phe750Ser
ENST00000343796.6:c.2246T>C	ENSP00000343205.2:p.Phe749Ser
ENST00000394464.6:c.2246T>C	ENSP00000377977.2:p.Phe749Ser
ENST00000394466.6:c.2249T>C	ENSP00000377979.2:p.Phe750Ser
ENST00000415690.6:c.2181+591T>C	ENSP00000387672.2:n.2181+591T>C
ENST00000424646.6:c.2168T>C	ENSP00000405282.2:p.Phe723Ser
ENST00000503201.1:c.2246T>C	ENSP00000427672.1:p.Phe749Ser
ENST00000504572.5:c.2249T>C	ENSP00000422518.1:p.Phe750Ser
NM_000176.2:c.2246T>C	NP_000167.1:p.Phe749Ser
NM_001018074.1:c.2246T>C	NP_001018084.1:p.Phe749Ser
NM_001018075.1:c.2246T>C	NP_001018085.1:p.Phe749Ser
NM_001018076.1:c.2246T>C	NP_001018086.1:p.Phe749Ser
NM_001018077.1:c.2246T>C	NP_001018087.1:p.Phe749Ser
NM_001020825.1:c.2181+591T>C	NP_001018661.1:n.2181+591T>C
NM_001024094.1:c.2249T>C	NP_001019265.1:p.Phe750Ser
NM_001204258.1:c.2168T>C	NP_001191187.1:p.Phe723Ser
NM_001204259.1:c.1991T>C	NP_001191188.1:p.Phe664Ser
NM_001204260.1:c.1979T>C	NP_001191189.1:p.Phe660Ser
NM_001204261.1:c.1955T>C	NP_001191190.1:p.Phe652Ser
NM_001204262.1:c.1301T>C	NP_001191191.1:p.Phe434Ser
NM_001204263.1:c.1256T>C	NP_001191192.1:p.Phe419Ser
NM_001204264.1:c.1241T>C	NP_001191193.1:p.Phe414Ser
XM_005268419.2:c.2249T>C	XP_005268476.1:p.Phe750Ser
XM_005268420.3:c.2249T>C	XP_005268477.1:p.Phe750Ser
XM_005268422.2:c.2249T>C	XP_005268479.1:p.Phe750Ser
XM_005268423.2:c.2249T>C	XP_005268480.1:p.Phe750Ser
XM_011537637.1:c.1055T>C	XP_011535939.1:p.Phe352Ser
XR_944371.1:n.656-2722A>G
NR_157096.1:n.1169T>C
XM_005268419.4:c.2249T>C	XP_005268476.1:p.Phe750Ser
XM_005268420.4:c.2249T>C	XP_005268477.1:p.Phe750Ser
XM_005268422.3:c.2249T>C	XP_005268479.1:p.Phe750Ser
XM_005268423.3:c.2249T>C	XP_005268480.1:p.Phe750Ser
XM_011537637.3:c.1055T>C	XP_011535939.1:p.Phe352Ser
XM_017009397.1:c.2246T>C	XP_016864886.1:p.Phe749Ser
XM_017009398.1:c.2246T>C	XP_016864887.1:p.Phe749Ser
NM_000176.3:c.2246T>C MANE Select	NP_000167.1:p.Phe749Ser
NM_001364180.1:c.2246T>C	NP_001351109.1:p.Phe749Ser
NM_001364181.1:c.2246T>C	NP_001351110.1:p.Phe749Ser
NM_001364182.1:c.2246T>C	NP_001351111.1:p.Phe749Ser
NM_001364183.1:c.2249T>C	NP_001351112.1:p.Phe750Ser
NM_001364184.1:c.2249T>C	NP_001351113.1:p.Phe750Ser
NM_001364185.1:c.2249T>C	NP_001351114.1:p.Phe750Ser
NM_001018076.2:c.2246T>C	NP_001018086.1:p.Phe749Ser
NM_001020825.2:c.2181+591T>C	NP_001018661.1:n.2181+591T>C
NM_001024094.2:c.2249T>C	NP_001019265.1:p.Phe750Ser
NM_001204258.2:c.2168T>C	NP_001191187.1:p.Phe723Ser
NM_001204259.2:c.1991T>C	NP_001191188.1:p.Phe664Ser
NM_001204260.2:c.1979T>C	NP_001191189.1:p.Phe660Ser
NM_001204261.2:c.1955T>C	NP_001191190.1:p.Phe652Ser
NM_001204262.2:c.1301T>C	NP_001191191.1:p.Phe434Ser
NM_001204263.2:c.1256T>C	NP_001191192.1:p.Phe419Ser
NM_001204264.2:c.1241T>C	NP_001191193.1:p.Phe414Ser
NM_001364180.2:c.2246T>C	NP_001351109.1:p.Phe749Ser
NM_001364181.2:c.2246T>C	NP_001351110.1:p.Phe749Ser
NM_001364183.2:c.2249T>C	NP_001351112.1:p.Phe750Ser
NM_001364184.2:c.2249T>C	NP_001351113.1:p.Phe750Ser
NR_157096.2:n.1169T>C