Canonical Allele Identifier: CA117246

Gene: FOXP2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114642616C>T , CM000669.2:g.114642616C>T	GRCh38
NC_000007.13:g.114282671C>T , CM000669.1:g.114282671C>T	GRCh37
NC_000007.12:g.114069907C>T	NCBI36
NG_007491.2:g.561307C>T
NG_007491.3:g.561307C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1033C>T	ENSP00000385069.4:p.Arg345Ter
ENST00000703612.1:c.973C>T	ENSP00000515396.1:p.Arg325Ter
ENST00000703613.1:c.1033C>T	ENSP00000515397.1:p.Arg345Ter
ENST00000703614.1:c.982C>T	ENSP00000515398.1:p.Arg328Ter
ENST00000703616.1:c.1108C>T	ENSP00000515400.1:p.Arg370Ter
ENST00000703617.1:c.706C>T	ENSP00000515401.1:p.Arg236Ter
ENST00000703618.1:c.260C>T
ENST00000350908.9:c.982C>T MANE Select	ENSP00000265436.7:p.Arg328Ter
ENST00000393489.8:c.*776C>T	ENSP00000377129.4:n.*776C>T
ENST00000350908.8:c.982C>T	ENSP00000265436.7:p.Arg328Ter
ENST00000360232.8:c.982C>T	ENSP00000353367.4:p.Arg328Ter
ENST00000378237.7:c.982C>T	ENSP00000367482.3:p.Arg328Ter
ENST00000390668.3:c.1054C>T	ENSP00000375084.3:p.Arg352Ter
ENST00000393489.7:c.706C>T	ENSP00000377129.3:p.Arg236Ter
ENST00000393491.7:c.706C>T	ENSP00000377130.3:p.Arg236Ter
ENST00000393494.6:c.982C>T	ENSP00000377132.2:p.Arg328Ter
ENST00000393498.6:c.919C>T	ENSP00000377135.2:p.Arg307Ter
ENST00000403559.8:c.1033C>T	ENSP00000385069.4:p.Arg345Ter
ENST00000408937.7:c.1057C>T	ENSP00000386200.3:p.Arg353Ter
ENST00000412402.5:c.*902C>T	ENSP00000405470.1:n.*902C>T
ENST00000441290.6:c.*827C>T	ENSP00000416825.1:n.*827C>T
ENST00000634372.1:n.222-9587C>T
ENST00000634411.1:c.931C>T	ENSP00000489135.1:p.Arg311Ter
ENST00000634623.1:c.922C>T	ENSP00000488944.1:p.Arg308Ter
ENST00000635109.1:c.*779C>T	ENSP00000489457.1:n.*779C>T
ENST00000635534.1:c.973C>T	ENSP00000489229.1:p.Arg325Ter
ENST00000635563.1:c.522C>T
ENST00000635638.1:c.985C>T	ENSP00000489073.1:p.Arg329Ter
NM_001172766.2:c.979C>T	NP_001166237.1:p.Arg327Ter
NM_001172767.2:c.1057C>T	NP_001166238.1:p.Arg353Ter
NM_014491.3:c.982C>T	NP_055306.1:p.Arg328Ter
NM_148898.3:c.1057C>T	NP_683696.2:p.Arg353Ter
NM_148899.3:c.982C>T	NP_683697.2:p.Arg328Ter
NM_148900.3:c.1033C>T	NP_683698.2:p.Arg345Ter
NR_033766.1:n.1569C>T
NR_033767.1:n.1414C>T
XM_011516706.1:c.1126C>T	XP_011515008.1:p.Arg376Ter
XM_017012801.2:c.1057C>T	XP_016868290.1:p.Arg353Ter
NM_014491.4:c.982C>T MANE Select	NP_055306.1:p.Arg328Ter
NM_001172766.3:c.979C>T	NP_001166237.1:p.Arg327Ter
NM_148898.4:c.1057C>T	NP_683696.2:p.Arg353Ter
NR_033766.2:n.1552C>T
NR_033767.2:n.1596C>T
NM_148900.4:c.1033C>T	NP_683698.2:p.Arg345Ter