Canonical Allele Identifier: CA368965718

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299723T>C (hg19) ; chr7:g.114659668T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659668T>C , CM000669.2:g.114659668T>C	GRCh38
NC_000007.13:g.114299723T>C , CM000669.1:g.114299723T>C	GRCh37
NC_000007.12:g.114086959T>C	NCBI36
NG_007491.2:g.578359T>C
NG_007491.3:g.578359T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1693T>C	ENSP00000385069.4:p.Trp565Arg
ENST00000703612.1:c.1633T>C	ENSP00000515396.1:p.Trp545Arg
ENST00000703613.1:c.1693T>C	ENSP00000515397.1:p.Trp565Arg
ENST00000703614.1:c.1642T>C	ENSP00000515398.1:p.Trp548Arg
ENST00000703616.1:c.1768T>C	ENSP00000515400.1:p.Trp590Arg
ENST00000703617.1:c.1087T>C	ENSP00000515401.1:p.Trp363Arg
ENST00000703618.1:c.545-2397T>C
ENST00000350908.9:c.1642T>C MANE Select	ENSP00000265436.7:p.Trp548Arg
ENST00000393489.8:c.*1436T>C	ENSP00000377129.4:n.*1436T>C
ENST00000350908.8:c.1642T>C	ENSP00000265436.7:p.Trp548Arg
ENST00000393489.7:c.1366T>C	ENSP00000377129.3:p.Trp456Arg
ENST00000393491.7:c.1087T>C	ENSP00000377130.3:p.Trp363Arg
ENST00000393494.6:c.1642T>C	ENSP00000377132.2:p.Trp548Arg
ENST00000393498.6:c.1579T>C	ENSP00000377135.2:p.Trp527Arg
ENST00000403559.8:c.1693T>C	ENSP00000385069.4:p.Trp565Arg
ENST00000408937.7:c.1717T>C	ENSP00000386200.3:p.Trp573Arg
ENST00000412402.5:c.*1360T>C	ENSP00000405470.1:n.*1360T>C
ENST00000441290.6:c.*1642T>C	ENSP00000416825.1:n.*1642T>C
ENST00000634411.1:c.1591T>C	ENSP00000489135.1:p.Trp531Arg
ENST00000634623.1:c.1582T>C	ENSP00000488944.1:p.Trp528Arg
ENST00000635109.1:c.*1439T>C	ENSP00000489457.1:n.*1439T>C
ENST00000635534.1:c.1633T>C	ENSP00000489229.1:p.Trp545Arg
ENST00000635638.1:c.1645T>C	ENSP00000489073.1:p.Trp549Arg
NM_001172766.2:c.1639T>C	NP_001166237.1:p.Trp547Arg
NM_014491.3:c.1642T>C	NP_055306.1:p.Trp548Arg
NM_148898.3:c.1717T>C	NP_683696.2:p.Trp573Arg
NM_148900.3:c.1693T>C	NP_683698.2:p.Trp565Arg
NR_033766.1:n.2027T>C
NR_033767.1:n.2074T>C
XM_011516706.1:c.1786T>C	XP_011515008.1:p.Trp596Arg
XM_017012801.2:c.1717T>C	XP_016868290.1:p.Trp573Arg
NM_014491.4:c.1642T>C MANE Select	NP_055306.1:p.Trp548Arg
NM_001172766.3:c.1639T>C	NP_001166237.1:p.Trp547Arg
NM_148898.4:c.1717T>C	NP_683696.2:p.Trp573Arg
NR_033766.2:n.2010T>C
NR_033767.2:n.2256T>C
NM_148900.4:c.1693T>C	NP_683698.2:p.Trp565Arg