Canonical Allele Identifier: CA361869108

Gene: NR3C1

Linked Data

• MyVariant Identifiers: chr5:g.142662287G>T (hg19) ; chr5:g.143282722G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143282722G>T , CM000667.2:g.143282722G>T	GRCh38
NC_000005.9:g.142662287G>T , CM000667.1:g.142662287G>T	GRCh37
NC_000005.8:g.142642480G>T	NCBI36
NG_009062.1:g.157791C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394464.7:c.2027C>A MANE Select	ENSP00000377977.2:p.Pro676His
ENST00000652686.1:c.1934C>A	ENSP00000498663.1:p.Pro645His
ENST00000231509.7:c.2030C>A	ENSP00000231509.3:p.Pro677His
ENST00000343796.6:c.2027C>A	ENSP00000343205.2:p.Pro676His
ENST00000394464.6:c.2027C>A	ENSP00000377977.2:p.Pro676His
ENST00000394466.6:c.2030C>A	ENSP00000377979.2:p.Pro677His
ENST00000415690.6:c.2027C>A	ENSP00000387672.2:p.Pro676His
ENST00000424646.6:c.1949C>A	ENSP00000405282.2:p.Pro650His
ENST00000503201.1:c.2027C>A	ENSP00000427672.1:p.Pro676His
ENST00000504572.5:c.2030C>A	ENSP00000422518.1:p.Pro677His
NM_000176.2:c.2027C>A	NP_000167.1:p.Pro676His
NM_001018074.1:c.2027C>A	NP_001018084.1:p.Pro676His
NM_001018075.1:c.2027C>A	NP_001018085.1:p.Pro676His
NM_001018076.1:c.2027C>A	NP_001018086.1:p.Pro676His
NM_001018077.1:c.2027C>A	NP_001018087.1:p.Pro676His
NM_001020825.1:c.2027C>A	NP_001018661.1:p.Pro676His
NM_001024094.1:c.2030C>A	NP_001019265.1:p.Pro677His
NM_001204258.1:c.1949C>A	NP_001191187.1:p.Pro650His
NM_001204259.1:c.1772C>A	NP_001191188.1:p.Pro591His
NM_001204260.1:c.1760C>A	NP_001191189.1:p.Pro587His
NM_001204261.1:c.1736C>A	NP_001191190.1:p.Pro579His
NM_001204262.1:c.1082C>A	NP_001191191.1:p.Pro361His
NM_001204263.1:c.1037C>A	NP_001191192.1:p.Pro346His
NM_001204264.1:c.1022C>A	NP_001191193.1:p.Pro341His
XM_005268419.2:c.2030C>A	XP_005268476.1:p.Pro677His
XM_005268420.3:c.2030C>A	XP_005268477.1:p.Pro677His
XM_005268422.2:c.2030C>A	XP_005268479.1:p.Pro677His
XM_005268423.2:c.2030C>A	XP_005268480.1:p.Pro677His
XM_011537637.1:c.836C>A	XP_011535939.1:p.Pro279His
XR_944371.1:n.656-1977G>T
NR_157096.1:n.950C>A
XM_005268419.4:c.2030C>A	XP_005268476.1:p.Pro677His
XM_005268420.4:c.2030C>A	XP_005268477.1:p.Pro677His
XM_005268422.3:c.2030C>A	XP_005268479.1:p.Pro677His
XM_005268423.3:c.2030C>A	XP_005268480.1:p.Pro677His
XM_011537637.3:c.836C>A	XP_011535939.1:p.Pro279His
XM_017009397.1:c.2027C>A	XP_016864886.1:p.Pro676His
XM_017009398.1:c.2027C>A	XP_016864887.1:p.Pro676His
NM_000176.3:c.2027C>A MANE Select	NP_000167.1:p.Pro676His
NM_001364180.1:c.2027C>A	NP_001351109.1:p.Pro676His
NM_001364181.1:c.2027C>A	NP_001351110.1:p.Pro676His
NM_001364182.1:c.2027C>A	NP_001351111.1:p.Pro676His
NM_001364183.1:c.2030C>A	NP_001351112.1:p.Pro677His
NM_001364184.1:c.2030C>A	NP_001351113.1:p.Pro677His
NM_001364185.1:c.2030C>A	NP_001351114.1:p.Pro677His
NM_001018076.2:c.2027C>A	NP_001018086.1:p.Pro676His
NM_001020825.2:c.2027C>A	NP_001018661.1:p.Pro676His
NM_001024094.2:c.2030C>A	NP_001019265.1:p.Pro677His
NM_001204258.2:c.1949C>A	NP_001191187.1:p.Pro650His
NM_001204259.2:c.1772C>A	NP_001191188.1:p.Pro591His
NM_001204260.2:c.1760C>A	NP_001191189.1:p.Pro587His
NM_001204261.2:c.1736C>A	NP_001191190.1:p.Pro579His
NM_001204262.2:c.1082C>A	NP_001191191.1:p.Pro361His
NM_001204263.2:c.1037C>A	NP_001191192.1:p.Pro346His
NM_001204264.2:c.1022C>A	NP_001191193.1:p.Pro341His
NM_001364180.2:c.2027C>A	NP_001351109.1:p.Pro676His
NM_001364181.2:c.2027C>A	NP_001351110.1:p.Pro676His
NM_001364183.2:c.2030C>A	NP_001351112.1:p.Pro677His
NM_001364184.2:c.2030C>A	NP_001351113.1:p.Pro677His
NR_157096.2:n.950C>A