Canonical Allele Identifier: CA368965537

Gene: FOXP2

Linked Data

• dbSNP Id: rs1308658577
• MyVariant Identifiers: chr7:g.114299643C>T (hg19) ; chr7:g.114659588C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659588C>T , CM000669.2:g.114659588C>T	GRCh38
NC_000007.13:g.114299643C>T , CM000669.1:g.114299643C>T	GRCh37
NC_000007.12:g.114086879C>T	NCBI36
NG_007491.2:g.578279C>T
NG_007491.3:g.578279C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1613C>T	ENSP00000385069.4:p.Ser538Phe
ENST00000703612.1:c.1553C>T	ENSP00000515396.1:p.Ser518Phe
ENST00000703613.1:c.1613C>T	ENSP00000515397.1:p.Ser538Phe
ENST00000703614.1:c.1562C>T	ENSP00000515398.1:p.Ser521Phe
ENST00000703616.1:c.1688C>T	ENSP00000515400.1:p.Ser563Phe
ENST00000703617.1:c.1007C>T	ENSP00000515401.1:p.Ser336Phe
ENST00000703618.1:c.545-2477C>T
ENST00000350908.9:c.1562C>T MANE Select	ENSP00000265436.7:p.Ser521Phe
ENST00000393489.8:c.*1356C>T	ENSP00000377129.4:n.*1356C>T
ENST00000350908.8:c.1562C>T	ENSP00000265436.7:p.Ser521Phe
ENST00000393489.7:c.1286C>T	ENSP00000377129.3:p.Ser429Phe
ENST00000393491.7:c.1007C>T	ENSP00000377130.3:p.Ser336Phe
ENST00000393494.6:c.1562C>T	ENSP00000377132.2:p.Ser521Phe
ENST00000393498.6:c.1499C>T	ENSP00000377135.2:p.Ser500Phe
ENST00000403559.8:c.1613C>T	ENSP00000385069.4:p.Ser538Phe
ENST00000408937.7:c.1637C>T	ENSP00000386200.3:p.Ser546Phe
ENST00000412402.5:c.*1280C>T	ENSP00000405470.1:n.*1280C>T
ENST00000441290.6:c.*1562C>T	ENSP00000416825.1:n.*1562C>T
ENST00000634411.1:c.1511C>T	ENSP00000489135.1:p.Ser504Phe
ENST00000634623.1:c.1502C>T	ENSP00000488944.1:p.Ser501Phe
ENST00000635109.1:c.*1359C>T	ENSP00000489457.1:n.*1359C>T
ENST00000635534.1:c.1553C>T	ENSP00000489229.1:p.Ser518Phe
ENST00000635638.1:c.1565C>T	ENSP00000489073.1:p.Ser522Phe
NM_001172766.2:c.1559C>T	NP_001166237.1:p.Ser520Phe
NM_014491.3:c.1562C>T	NP_055306.1:p.Ser521Phe
NM_148898.3:c.1637C>T	NP_683696.2:p.Ser546Phe
NM_148900.3:c.1613C>T	NP_683698.2:p.Ser538Phe
NR_033766.1:n.1947C>T
NR_033767.1:n.1994C>T
XM_011516706.1:c.1706C>T	XP_011515008.1:p.Ser569Phe
XM_017012801.2:c.1637C>T	XP_016868290.1:p.Ser546Phe
NM_014491.4:c.1562C>T MANE Select	NP_055306.1:p.Ser521Phe
NM_001172766.3:c.1559C>T	NP_001166237.1:p.Ser520Phe
NM_148898.4:c.1637C>T	NP_683696.2:p.Ser546Phe
NR_033766.2:n.1930C>T
NR_033767.2:n.2176C>T
NM_148900.4:c.1613C>T	NP_683698.2:p.Ser538Phe