Canonical Allele Identifier: CA348679627

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182408G>A (hg19) ; chr2:g.156325896G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325896G>A , CM000664.2:g.156325896G>A	GRCh38
NC_000002.11:g.157182408G>A , CM000664.1:g.157182408G>A	GRCh37
NC_000002.10:g.156890654G>A	NCBI36
NG_011821.1:g.11880C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1441C>T	ENSP00000514865.1:p.Pro481Ser
ENST00000700229.1:c.609C>T
ENST00000700230.1:c.1185C>T	ENSP00000514867.1:n.1185C>T
ENST00000700231.1:c.1570C>T	ENSP00000514868.1:p.Pro524Ser
ENST00000339562.9:c.1645C>T MANE Select	ENSP00000344479.4:p.Pro549Ser
ENST00000675870.1:c.*156C>T	ENSP00000502739.1:n.*156C>T
ENST00000339562.8:c.1645C>T	ENSP00000344479.4:p.Pro549Ser
ENST00000409108.6:c.1541C>T	ENSP00000386993.2:p.Pro514Leu
ENST00000409572.5:c.1645C>T	ENSP00000386747.1:p.Pro549Ser
ENST00000417764.5:c.*156C>T	ENSP00000415632.1:n.*156C>T
ENST00000417972.5:c.*156C>T	ENSP00000394671.1:n.*156C>T
ENST00000426264.5:c.1456C>T	ENSP00000389986.1:p.Pro486Ser
ENST00000429376.5:c.1352C>T	ENSP00000410952.1:p.Pro451Leu
NM_006186.3:c.1645C>T	NP_006177.1:p.Pro549Ser
XM_005246621.2:c.1678C>T	XP_005246678.1:p.Pro560Ser
XM_005246622.2:c.1456C>T	XP_005246679.1:p.Pro486Ser
XM_005246623.1:c.1456C>T	XP_005246680.1:p.Pro486Ser
XM_006712553.2:c.1603C>T	XP_006712616.1:p.Pro535Ser
XM_011511246.1:c.1574C>T	XP_011509548.1:p.Pro525Leu
NM_173173.2:c.1456C>T	NP_775265.1:p.Pro486Ser
XM_005246621.4:c.1678C>T	XP_005246678.1:p.Pro560Ser
XM_006712553.4:c.1603C>T	XP_006712616.1:p.Pro535Ser
XM_011511246.2:c.1574C>T	XP_011509548.1:p.Pro525Leu
XM_017004219.2:c.1645C>T	XP_016859708.1:p.Pro549Ser
XM_017004220.2:c.1570C>T	XP_016859709.1:p.Pro524Ser
XR_001738751.2:n.1892C>T
XR_001738752.2:n.1714C>T
XR_427087.4:n.1771C>T
NM_006186.4:c.1645C>T MANE Select	NP_006177.1:p.Pro549Ser
NM_173173.3:c.1456C>T	NP_775265.1:p.Pro486Ser