Canonical Allele Identifier: CA368965774

Gene: FOXP2

Linked Data

• ClinVar Variation Id: 1710171
• ClinVar RCV Id: RCV002291098
• MyVariant Identifiers: chr7:g.114302133A>G (hg19) ; chr7:g.114662078A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662078A>G , CM000669.2:g.114662078A>G	GRCh38
NC_000007.13:g.114302133A>G , CM000669.1:g.114302133A>G	GRCh37
NC_000007.12:g.114089369A>G	NCBI36
NG_007491.2:g.580769A>G
NG_007491.3:g.580769A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1712A>G	ENSP00000385069.4:p.His571Arg
ENST00000703612.1:c.1652A>G	ENSP00000515396.1:p.His551Arg
ENST00000703613.1:c.1712A>G	ENSP00000515397.1:p.His571Arg
ENST00000703614.1:c.1661A>G	ENSP00000515398.1:p.His554Arg
ENST00000703616.1:c.1787A>G	ENSP00000515400.1:p.His596Arg
ENST00000703617.1:c.1106A>G	ENSP00000515401.1:p.His369Arg
ENST00000703618.1:c.558A>G
ENST00000350908.9:c.1661A>G MANE Select	ENSP00000265436.7:p.His554Arg
ENST00000393489.8:c.*1455A>G	ENSP00000377129.4:n.*1455A>G
ENST00000350908.8:c.1661A>G	ENSP00000265436.7:p.His554Arg
ENST00000393489.7:c.1385A>G	ENSP00000377129.3:p.His462Arg
ENST00000393491.7:c.1106A>G	ENSP00000377130.3:p.His369Arg
ENST00000393494.6:c.1661A>G	ENSP00000377132.2:p.His554Arg
ENST00000393498.6:c.1598A>G	ENSP00000377135.2:p.His533Arg
ENST00000403559.8:c.1712A>G	ENSP00000385069.4:p.His571Arg
ENST00000408937.7:c.1736A>G	ENSP00000386200.3:p.His579Arg
ENST00000412402.5:c.*1379A>G	ENSP00000405470.1:n.*1379A>G
ENST00000441290.6:c.*1661A>G	ENSP00000416825.1:n.*1661A>G
ENST00000634411.1:c.1610A>G	ENSP00000489135.1:p.His537Arg
ENST00000634623.1:c.1601A>G	ENSP00000488944.1:p.His534Arg
ENST00000634664.1:n.136A>G
ENST00000635109.1:c.*1458A>G	ENSP00000489457.1:n.*1458A>G
ENST00000635534.1:c.1652A>G	ENSP00000489229.1:p.His551Arg
ENST00000635638.1:c.1664A>G	ENSP00000489073.1:p.His555Arg
NM_001172766.2:c.1658A>G	NP_001166237.1:p.His553Arg
NM_014491.3:c.1661A>G	NP_055306.1:p.His554Arg
NM_148898.3:c.1736A>G	NP_683696.2:p.His579Arg
NM_148900.3:c.1712A>G	NP_683698.2:p.His571Arg
NR_033766.1:n.2046A>G
NR_033767.1:n.2093A>G
XM_011516706.1:c.1805A>G	XP_011515008.1:p.His602Arg
XM_017012801.2:c.1736A>G	XP_016868290.1:p.His579Arg
NM_014491.4:c.1661A>G MANE Select	NP_055306.1:p.His554Arg
NM_001172766.3:c.1658A>G	NP_001166237.1:p.His553Arg
NM_148898.4:c.1736A>G	NP_683696.2:p.His579Arg
NR_033766.2:n.2029A>G
NR_033767.2:n.2275A>G
NM_148900.4:c.1712A>G	NP_683698.2:p.His571Arg