Canonical Allele Identifier: CA368965877

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302178A>G (hg19) ; chr7:g.114662123A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662123A>G , CM000669.2:g.114662123A>G	GRCh38
NC_000007.13:g.114302178A>G , CM000669.1:g.114302178A>G	GRCh37
NC_000007.12:g.114089414A>G	NCBI36
NG_007491.2:g.580814A>G
NG_007491.3:g.580814A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1757A>G	ENSP00000385069.4:p.Lys586Arg
ENST00000703612.1:c.1697A>G	ENSP00000515396.1:p.Lys566Arg
ENST00000703613.1:c.1757A>G	ENSP00000515397.1:p.Lys586Arg
ENST00000703614.1:c.1706A>G	ENSP00000515398.1:p.Lys569Arg
ENST00000703616.1:c.1832A>G	ENSP00000515400.1:p.Lys611Arg
ENST00000703617.1:c.1151A>G	ENSP00000515401.1:p.Lys384Arg
ENST00000703618.1:c.603A>G
ENST00000350908.9:c.1706A>G MANE Select	ENSP00000265436.7:p.Lys569Arg
ENST00000393489.8:c.*1500A>G	ENSP00000377129.4:n.*1500A>G
ENST00000350908.8:c.1706A>G	ENSP00000265436.7:p.Lys569Arg
ENST00000393489.7:c.1430A>G	ENSP00000377129.3:p.Lys477Arg
ENST00000393491.7:c.1151A>G	ENSP00000377130.3:p.Lys384Arg
ENST00000393494.6:c.1706A>G	ENSP00000377132.2:p.Lys569Arg
ENST00000393498.6:c.1643A>G	ENSP00000377135.2:p.Lys548Arg
ENST00000403559.8:c.1757A>G	ENSP00000385069.4:p.Lys586Arg
ENST00000408937.7:c.1781A>G	ENSP00000386200.3:p.Lys594Arg
ENST00000412402.5:c.*1424A>G	ENSP00000405470.1:n.*1424A>G
ENST00000441290.6:c.*1706A>G	ENSP00000416825.1:n.*1706A>G
ENST00000634411.1:c.1655A>G	ENSP00000489135.1:p.Lys552Arg
ENST00000634623.1:c.1646A>G	ENSP00000488944.1:p.Lys549Arg
ENST00000634664.1:n.181A>G
ENST00000635109.1:c.*1503A>G	ENSP00000489457.1:n.*1503A>G
ENST00000635534.1:c.1697A>G	ENSP00000489229.1:p.Lys566Arg
ENST00000635638.1:c.1709A>G	ENSP00000489073.1:p.Lys570Arg
NM_001172766.2:c.1703A>G	NP_001166237.1:p.Lys568Arg
NM_014491.3:c.1706A>G	NP_055306.1:p.Lys569Arg
NM_148898.3:c.1781A>G	NP_683696.2:p.Lys594Arg
NM_148900.3:c.1757A>G	NP_683698.2:p.Lys586Arg
NR_033766.1:n.2091A>G
NR_033767.1:n.2138A>G
XM_011516706.1:c.1850A>G	XP_011515008.1:p.Lys617Arg
XM_017012801.2:c.1781A>G	XP_016868290.1:p.Lys594Arg
NM_014491.4:c.1706A>G MANE Select	NP_055306.1:p.Lys569Arg
NM_001172766.3:c.1703A>G	NP_001166237.1:p.Lys568Arg
NM_148898.4:c.1781A>G	NP_683696.2:p.Lys594Arg
NR_033766.2:n.2074A>G
NR_033767.2:n.2320A>G
NM_148900.4:c.1757A>G	NP_683698.2:p.Lys586Arg