Canonical Allele Identifier: CA368962897

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114631645C>T , CM000669.2:g.114631645C>T	GRCh38
NC_000007.13:g.114271700C>T , CM000669.1:g.114271700C>T	GRCh37
NC_000007.12:g.114058936C>T	NCBI36
NG_007491.2:g.550336C>T
NG_007491.3:g.550336C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.766C>T	ENSP00000385069.4:p.Gln256Ter
ENST00000703612.1:c.706C>T	ENSP00000515396.1:p.Gln236Ter
ENST00000703613.1:c.766C>T	ENSP00000515397.1:p.Gln256Ter
ENST00000703614.1:c.715C>T	ENSP00000515398.1:p.Gln239Ter
ENST00000703616.1:c.841C>T	ENSP00000515400.1:p.Gln281Ter
ENST00000703617.1:c.439C>T	ENSP00000515401.1:p.Gln147Ter
ENST00000350908.9:c.715C>T MANE Select	ENSP00000265436.7:p.Gln239Ter
ENST00000393489.8:c.*509C>T	ENSP00000377129.4:n.*509C>T
ENST00000350908.8:c.715C>T	ENSP00000265436.7:p.Gln239Ter
ENST00000360232.8:c.715C>T	ENSP00000353367.4:p.Gln239Ter
ENST00000378237.7:c.715C>T	ENSP00000367482.3:p.Gln239Ter
ENST00000390668.3:c.787C>T	ENSP00000375084.3:p.Gln263Ter
ENST00000393489.7:c.439C>T	ENSP00000377129.3:p.Gln147Ter
ENST00000393491.7:c.439C>T	ENSP00000377130.3:p.Gln147Ter
ENST00000393494.6:c.715C>T	ENSP00000377132.2:p.Gln239Ter
ENST00000393495.7:c.277C>T	ENSP00000377133.3:p.Gln93Ter
ENST00000393498.6:c.652C>T	ENSP00000377135.2:p.Gln218Ter
ENST00000403559.8:c.766C>T	ENSP00000385069.4:p.Gln256Ter
ENST00000408937.7:c.790C>T	ENSP00000386200.3:p.Gln264Ter
ENST00000412402.5:c.*635C>T	ENSP00000405470.1:n.*635C>T
ENST00000441290.6:c.*560C>T	ENSP00000416825.1:n.*560C>T
ENST00000634372.1:n.161C>T
ENST00000634411.1:c.664C>T	ENSP00000489135.1:p.Gln222Ter
ENST00000634623.1:c.655C>T	ENSP00000488944.1:p.Gln219Ter
ENST00000635109.1:c.*512C>T	ENSP00000489457.1:n.*512C>T
ENST00000635534.1:c.706C>T	ENSP00000489229.1:p.Gln236Ter
ENST00000635563.1:c.255C>T
ENST00000635638.1:c.718C>T	ENSP00000489073.1:p.Gln240Ter
NM_001172766.2:c.712C>T	NP_001166237.1:p.Gln238Ter
NM_001172767.2:c.790C>T	NP_001166238.1:p.Gln264Ter
NM_014491.3:c.715C>T	NP_055306.1:p.Gln239Ter
NM_148898.3:c.790C>T	NP_683696.2:p.Gln264Ter
NM_148899.3:c.715C>T	NP_683697.2:p.Gln239Ter
NM_148900.3:c.766C>T	NP_683698.2:p.Gln256Ter
NR_033766.1:n.1302C>T
NR_033767.1:n.1147C>T
XM_011516706.1:c.859C>T	XP_011515008.1:p.Gln287Ter
XM_017012801.2:c.790C>T	XP_016868290.1:p.Gln264Ter
NM_014491.4:c.715C>T MANE Select	NP_055306.1:p.Gln239Ter
NM_001172766.3:c.712C>T	NP_001166237.1:p.Gln238Ter
NM_148898.4:c.790C>T	NP_683696.2:p.Gln264Ter
NR_033766.2:n.1285C>T
NR_033767.2:n.1329C>T
NM_148900.4:c.766C>T	NP_683698.2:p.Gln256Ter