Canonical Allele Identifier: CA368965843

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662107C>T , CM000669.2:g.114662107C>T	GRCh38
NC_000007.13:g.114302162C>T , CM000669.1:g.114302162C>T	GRCh37
NC_000007.12:g.114089398C>T	NCBI36
NG_007491.2:g.580798C>T
NG_007491.3:g.580798C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1741C>T	ENSP00000385069.4:p.Arg581Ter
ENST00000703612.1:c.1681C>T	ENSP00000515396.1:p.Arg561Ter
ENST00000703613.1:c.1741C>T	ENSP00000515397.1:p.Arg581Ter
ENST00000703614.1:c.1690C>T	ENSP00000515398.1:p.Arg564Ter
ENST00000703616.1:c.1816C>T	ENSP00000515400.1:p.Arg606Ter
ENST00000703617.1:c.1135C>T	ENSP00000515401.1:p.Arg379Ter
ENST00000703618.1:c.587C>T
ENST00000350908.9:c.1690C>T MANE Select	ENSP00000265436.7:p.Arg564Ter
ENST00000393489.8:c.*1484C>T	ENSP00000377129.4:n.*1484C>T
ENST00000350908.8:c.1690C>T	ENSP00000265436.7:p.Arg564Ter
ENST00000393489.7:c.1414C>T	ENSP00000377129.3:p.Arg472Ter
ENST00000393491.7:c.1135C>T	ENSP00000377130.3:p.Arg379Ter
ENST00000393494.6:c.1690C>T	ENSP00000377132.2:p.Arg564Ter
ENST00000393498.6:c.1627C>T	ENSP00000377135.2:p.Arg543Ter
ENST00000403559.8:c.1741C>T	ENSP00000385069.4:p.Arg581Ter
ENST00000408937.7:c.1765C>T	ENSP00000386200.3:p.Arg589Ter
ENST00000412402.5:c.*1408C>T	ENSP00000405470.1:n.*1408C>T
ENST00000441290.6:c.*1690C>T	ENSP00000416825.1:n.*1690C>T
ENST00000634411.1:c.1639C>T	ENSP00000489135.1:p.Arg547Ter
ENST00000634623.1:c.1630C>T	ENSP00000488944.1:p.Arg544Ter
ENST00000634664.1:n.165C>T
ENST00000635109.1:c.*1487C>T	ENSP00000489457.1:n.*1487C>T
ENST00000635534.1:c.1681C>T	ENSP00000489229.1:p.Arg561Ter
ENST00000635638.1:c.1693C>T	ENSP00000489073.1:p.Arg565Ter
NM_001172766.2:c.1687C>T	NP_001166237.1:p.Arg563Ter
NM_014491.3:c.1690C>T	NP_055306.1:p.Arg564Ter
NM_148898.3:c.1765C>T	NP_683696.2:p.Arg589Ter
NM_148900.3:c.1741C>T	NP_683698.2:p.Arg581Ter
NR_033766.1:n.2075C>T
NR_033767.1:n.2122C>T
XM_011516706.1:c.1834C>T	XP_011515008.1:p.Arg612Ter
XM_017012801.2:c.1765C>T	XP_016868290.1:p.Arg589Ter
NM_014491.4:c.1690C>T MANE Select	NP_055306.1:p.Arg564Ter
NM_001172766.3:c.1687C>T	NP_001166237.1:p.Arg563Ter
NM_148898.4:c.1765C>T	NP_683696.2:p.Arg589Ter
NR_033766.2:n.2058C>T
NR_033767.2:n.2304C>T
NM_148900.4:c.1741C>T	NP_683698.2:p.Arg581Ter