Canonical Allele Identifier: CA368965562

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299654T>G (hg19) ; chr7:g.114659599T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659599T>G , CM000669.2:g.114659599T>G	GRCh38
NC_000007.13:g.114299654T>G , CM000669.1:g.114299654T>G	GRCh37
NC_000007.12:g.114086890T>G	NCBI36
NG_007491.2:g.578290T>G
NG_007491.3:g.578290T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1624T>G	ENSP00000385069.4:p.Leu542Val
ENST00000703612.1:c.1564T>G	ENSP00000515396.1:p.Leu522Val
ENST00000703613.1:c.1624T>G	ENSP00000515397.1:p.Leu542Val
ENST00000703614.1:c.1573T>G	ENSP00000515398.1:p.Leu525Val
ENST00000703616.1:c.1699T>G	ENSP00000515400.1:p.Leu567Val
ENST00000703617.1:c.1018T>G	ENSP00000515401.1:p.Leu340Val
ENST00000703618.1:c.545-2466T>G
ENST00000350908.9:c.1573T>G MANE Select	ENSP00000265436.7:p.Leu525Val
ENST00000393489.8:c.*1367T>G	ENSP00000377129.4:n.*1367T>G
ENST00000350908.8:c.1573T>G	ENSP00000265436.7:p.Leu525Val
ENST00000393489.7:c.1297T>G	ENSP00000377129.3:p.Leu433Val
ENST00000393491.7:c.1018T>G	ENSP00000377130.3:p.Leu340Val
ENST00000393494.6:c.1573T>G	ENSP00000377132.2:p.Leu525Val
ENST00000393498.6:c.1510T>G	ENSP00000377135.2:p.Leu504Val
ENST00000403559.8:c.1624T>G	ENSP00000385069.4:p.Leu542Val
ENST00000408937.7:c.1648T>G	ENSP00000386200.3:p.Leu550Val
ENST00000412402.5:c.*1291T>G	ENSP00000405470.1:n.*1291T>G
ENST00000441290.6:c.*1573T>G	ENSP00000416825.1:n.*1573T>G
ENST00000634411.1:c.1522T>G	ENSP00000489135.1:p.Leu508Val
ENST00000634623.1:c.1513T>G	ENSP00000488944.1:p.Leu505Val
ENST00000635109.1:c.*1370T>G	ENSP00000489457.1:n.*1370T>G
ENST00000635534.1:c.1564T>G	ENSP00000489229.1:p.Leu522Val
ENST00000635638.1:c.1576T>G	ENSP00000489073.1:p.Leu526Val
NM_001172766.2:c.1570T>G	NP_001166237.1:p.Leu524Val
NM_014491.3:c.1573T>G	NP_055306.1:p.Leu525Val
NM_148898.3:c.1648T>G	NP_683696.2:p.Leu550Val
NM_148900.3:c.1624T>G	NP_683698.2:p.Leu542Val
NR_033766.1:n.1958T>G
NR_033767.1:n.2005T>G
XM_011516706.1:c.1717T>G	XP_011515008.1:p.Leu573Val
XM_017012801.2:c.1648T>G	XP_016868290.1:p.Leu550Val
NM_014491.4:c.1573T>G MANE Select	NP_055306.1:p.Leu525Val
NM_001172766.3:c.1570T>G	NP_001166237.1:p.Leu524Val
NM_148898.4:c.1648T>G	NP_683696.2:p.Leu550Val
NR_033766.2:n.1941T>G
NR_033767.2:n.2187T>G
NM_148900.4:c.1624T>G	NP_683698.2:p.Leu542Val