Canonical Allele Identifier: CA368965885

Gene: FOXP2

Linked Data

• COSMIC: COSM4531396 ; COSM4531397
• MyVariant Identifiers: chr7:g.114302181G>A (hg19) ; chr7:g.114662126G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662126G>A , CM000669.2:g.114662126G>A	GRCh38
NC_000007.13:g.114302181G>A , CM000669.1:g.114302181G>A	GRCh37
NC_000007.12:g.114089417G>A	NCBI36
NG_007491.2:g.580817G>A
NG_007491.3:g.580817G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1760G>A	ENSP00000385069.4:p.Gly587Glu
ENST00000703612.1:c.1700G>A	ENSP00000515396.1:p.Gly567Glu
ENST00000703613.1:c.1760G>A	ENSP00000515397.1:p.Gly587Glu
ENST00000703614.1:c.1709G>A	ENSP00000515398.1:p.Gly570Glu
ENST00000703616.1:c.1835G>A	ENSP00000515400.1:p.Gly612Glu
ENST00000703617.1:c.1154G>A	ENSP00000515401.1:p.Gly385Glu
ENST00000703618.1:c.606G>A
ENST00000350908.9:c.1709G>A MANE Select	ENSP00000265436.7:p.Gly570Glu
ENST00000393489.8:c.*1503G>A	ENSP00000377129.4:n.*1503G>A
ENST00000350908.8:c.1709G>A	ENSP00000265436.7:p.Gly570Glu
ENST00000393489.7:c.1433G>A	ENSP00000377129.3:p.Gly478Glu
ENST00000393491.7:c.1154G>A	ENSP00000377130.3:p.Gly385Glu
ENST00000393494.6:c.1709G>A	ENSP00000377132.2:p.Gly570Glu
ENST00000393498.6:c.1646G>A	ENSP00000377135.2:p.Gly549Glu
ENST00000403559.8:c.1760G>A	ENSP00000385069.4:p.Gly587Glu
ENST00000408937.7:c.1784G>A	ENSP00000386200.3:p.Gly595Glu
ENST00000412402.5:c.*1427G>A	ENSP00000405470.1:n.*1427G>A
ENST00000441290.6:c.*1709G>A	ENSP00000416825.1:n.*1709G>A
ENST00000634411.1:c.1658G>A	ENSP00000489135.1:p.Gly553Glu
ENST00000634623.1:c.1649G>A	ENSP00000488944.1:p.Gly550Glu
ENST00000634664.1:n.184G>A
ENST00000635109.1:c.*1506G>A	ENSP00000489457.1:n.*1506G>A
ENST00000635534.1:c.1700G>A	ENSP00000489229.1:p.Gly567Glu
ENST00000635638.1:c.1712G>A	ENSP00000489073.1:p.Gly571Glu
NM_001172766.2:c.1706G>A	NP_001166237.1:p.Gly569Glu
NM_014491.3:c.1709G>A	NP_055306.1:p.Gly570Glu
NM_148898.3:c.1784G>A	NP_683696.2:p.Gly595Glu
NM_148900.3:c.1760G>A	NP_683698.2:p.Gly587Glu
NR_033766.1:n.2094G>A
NR_033767.1:n.2141G>A
XM_011516706.1:c.1853G>A	XP_011515008.1:p.Gly618Glu
XM_017012801.2:c.1784G>A	XP_016868290.1:p.Gly595Glu
NM_014491.4:c.1709G>A MANE Select	NP_055306.1:p.Gly570Glu
NM_001172766.3:c.1706G>A	NP_001166237.1:p.Gly569Glu
NM_148898.4:c.1784G>A	NP_683696.2:p.Gly595Glu
NR_033766.2:n.2077G>A
NR_033767.2:n.2323G>A
NM_148900.4:c.1760G>A	NP_683698.2:p.Gly587Glu