Canonical Allele Identifier: CA1916209

Gene: NR4A2

Linked Data

• dbSNP Id: rs142345639
• ExAC: 2:157182707 C / T
• gnomAD v2: 2-157182707-C-T
• gnomAD v3: 2-156326195-C-T
• gnomAD v4: 2-156326195-C-T
• COSMIC: COSM1007973
• MyVariant Identifiers: chr2:g.157182707C>T (hg19) ; chr2:g.156326195C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326195C>T , CM000664.2:g.156326195C>T	GRCh38
NC_000002.11:g.157182707C>T , CM000664.1:g.157182707C>T	GRCh37
NC_000002.10:g.156890953C>T	NCBI36
NG_011821.1:g.11581G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1291G>A	ENSP00000514865.1:p.Asp431Asn
ENST00000700229.1:c.459G>A
ENST00000700230.1:c.1035G>A	ENSP00000514867.1:n.1035G>A
ENST00000700231.1:c.1420G>A	ENSP00000514868.1:p.Asp474Asn
ENST00000339562.9:c.1495G>A MANE Select	ENSP00000344479.4:p.Asp499Asn
ENST00000675870.1:c.*6G>A	ENSP00000502739.1:n.*6G>A
ENST00000339562.8:c.1495G>A	ENSP00000344479.4:p.Asp499Asn
ENST00000409108.6:c.1391G>A	ENSP00000386993.2:p.Arg464Gln
ENST00000409572.5:c.1495G>A	ENSP00000386747.1:p.Asp499Asn
ENST00000417764.5:c.*6G>A	ENSP00000415632.1:n.*6G>A
ENST00000417972.5:c.*6G>A	ENSP00000394671.1:n.*6G>A
ENST00000426264.5:c.1306G>A	ENSP00000389986.1:p.Asp436Asn
ENST00000429376.5:c.1202G>A	ENSP00000410952.1:p.Arg401Gln
NM_006186.3:c.1495G>A	NP_006177.1:p.Asp499Asn
XM_005246621.2:c.1528G>A	XP_005246678.1:p.Asp510Asn
XM_005246622.2:c.1306G>A	XP_005246679.1:p.Asp436Asn
XM_005246623.1:c.1306G>A	XP_005246680.1:p.Asp436Asn
XM_006712553.2:c.1453G>A	XP_006712616.1:p.Asp485Asn
XM_011511246.1:c.1424G>A	XP_011509548.1:p.Arg475Gln
XR_427087.2:n.3580G>A
NM_173173.2:c.1306G>A	NP_775265.1:p.Asp436Asn
XM_005246621.4:c.1528G>A	XP_005246678.1:p.Asp510Asn
XM_006712553.4:c.1453G>A	XP_006712616.1:p.Asp485Asn
XM_011511246.2:c.1424G>A	XP_011509548.1:p.Arg475Gln
XM_017004219.2:c.1495G>A	XP_016859708.1:p.Asp499Asn
XM_017004220.2:c.1420G>A	XP_016859709.1:p.Asp474Asn
XR_001738751.2:n.1742G>A
XR_001738752.2:n.1564G>A
XR_427087.4:n.1621G>A
NM_006186.4:c.1495G>A MANE Select	NP_006177.1:p.Asp499Asn
NM_173173.3:c.1306G>A	NP_775265.1:p.Asp436Asn