Canonical Allele Identifier: CA368965791

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302139T>G (hg19) ; chr7:g.114662084T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662084T>G , CM000669.2:g.114662084T>G	GRCh38
NC_000007.13:g.114302139T>G , CM000669.1:g.114302139T>G	GRCh37
NC_000007.12:g.114089375T>G	NCBI36
NG_007491.2:g.580775T>G
NG_007491.3:g.580775T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1718T>G	ENSP00000385069.4:p.Leu573Arg
ENST00000703612.1:c.1658T>G	ENSP00000515396.1:p.Leu553Arg
ENST00000703613.1:c.1718T>G	ENSP00000515397.1:p.Leu573Arg
ENST00000703614.1:c.1667T>G	ENSP00000515398.1:p.Leu556Arg
ENST00000703616.1:c.1793T>G	ENSP00000515400.1:p.Leu598Arg
ENST00000703617.1:c.1112T>G	ENSP00000515401.1:p.Leu371Arg
ENST00000703618.1:c.564T>G
ENST00000350908.9:c.1667T>G MANE Select	ENSP00000265436.7:p.Leu556Arg
ENST00000393489.8:c.*1461T>G	ENSP00000377129.4:n.*1461T>G
ENST00000350908.8:c.1667T>G	ENSP00000265436.7:p.Leu556Arg
ENST00000393489.7:c.1391T>G	ENSP00000377129.3:p.Leu464Arg
ENST00000393491.7:c.1112T>G	ENSP00000377130.3:p.Leu371Arg
ENST00000393494.6:c.1667T>G	ENSP00000377132.2:p.Leu556Arg
ENST00000393498.6:c.1604T>G	ENSP00000377135.2:p.Leu535Arg
ENST00000403559.8:c.1718T>G	ENSP00000385069.4:p.Leu573Arg
ENST00000408937.7:c.1742T>G	ENSP00000386200.3:p.Leu581Arg
ENST00000412402.5:c.*1385T>G	ENSP00000405470.1:n.*1385T>G
ENST00000441290.6:c.*1667T>G	ENSP00000416825.1:n.*1667T>G
ENST00000634411.1:c.1616T>G	ENSP00000489135.1:p.Leu539Arg
ENST00000634623.1:c.1607T>G	ENSP00000488944.1:p.Leu536Arg
ENST00000634664.1:n.142T>G
ENST00000635109.1:c.*1464T>G	ENSP00000489457.1:n.*1464T>G
ENST00000635534.1:c.1658T>G	ENSP00000489229.1:p.Leu553Arg
ENST00000635638.1:c.1670T>G	ENSP00000489073.1:p.Leu557Arg
NM_001172766.2:c.1664T>G	NP_001166237.1:p.Leu555Arg
NM_014491.3:c.1667T>G	NP_055306.1:p.Leu556Arg
NM_148898.3:c.1742T>G	NP_683696.2:p.Leu581Arg
NM_148900.3:c.1718T>G	NP_683698.2:p.Leu573Arg
NR_033766.1:n.2052T>G
NR_033767.1:n.2099T>G
XM_011516706.1:c.1811T>G	XP_011515008.1:p.Leu604Arg
XM_017012801.2:c.1742T>G	XP_016868290.1:p.Leu581Arg
NM_014491.4:c.1667T>G MANE Select	NP_055306.1:p.Leu556Arg
NM_001172766.3:c.1664T>G	NP_001166237.1:p.Leu555Arg
NM_148898.4:c.1742T>G	NP_683696.2:p.Leu581Arg
NR_033766.2:n.2035T>G
NR_033767.2:n.2281T>G
NM_148900.4:c.1718T>G	NP_683698.2:p.Leu573Arg