Canonical Allele Identifier: CA1736048465

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114663469A= , CM000669.2:g.114663469A=	GRCh38
NC_000007.13:g.114303524A= , CM000669.1:g.114303524A=	GRCh37
NC_000007.12:g.114090760A=	NCBI36
NG_007491.2:g.582160A=
NG_007491.3:g.582160A=

Transcript Alleles

HGVS	Amino-acid Change
NM_014491.4:c.1789A= MANE Select	NP_055306.1:p.Asn597=
ENST00000350908.9:c.1789A= MANE Select	ENSP00000265436.7:p.Asn597=
NM_001172766.2:c.1786A=	NP_001166237.1:p.Asn596=
NM_001172766.3:c.1786A=	NP_001166237.1:p.Asn596=
NM_014491.3:c.1789A=	NP_055306.1:p.Asn597=
NM_148898.3:c.1864A=	NP_683696.2:p.Asn622=
NM_148898.4:c.1864A=	NP_683696.2:p.Asn622=
NM_148900.3:c.1840A=	NP_683698.2:p.Asn614=
NM_148900.4:c.1840A=	NP_683698.2:p.Asn614=
NR_033766.1:n.2174A=
NR_033766.2:n.2157A=
NR_033767.1:n.2221A=
NR_033767.2:n.2403A=
ENST00000350908.8:c.1789A=	ENSP00000265436.7:p.Asn597=
ENST00000393489.7:c.1513A=	ENSP00000377129.3:p.Asn505=
ENST00000393489.8:c.*1583A=	ENSP00000377129.4:n.*1583A=
ENST00000393491.7:c.1234A=	ENSP00000377130.3:p.Asn412=
ENST00000393494.6:c.1789A=	ENSP00000377132.2:p.Asn597=
ENST00000393498.6:c.1726A=	ENSP00000377135.2:p.Asn576=
ENST00000403559.8:c.1840A=	ENSP00000385069.4:p.Asn614=
ENST00000403559.9:c.1840A=	ENSP00000385069.4:p.Asn614=
ENST00000408937.7:c.1864A=	ENSP00000386200.3:p.Asn622=
ENST00000412402.5:c.*1507A=	ENSP00000405470.1:n.*1507A=
ENST00000441290.6:c.*1789A=	ENSP00000416825.1:n.*1789A=
ENST00000634411.1:c.1738A=	ENSP00000489135.1:p.Asn580=
ENST00000634623.1:c.1729A=	ENSP00000488944.1:p.Asn577=
ENST00000634664.1:n.264A=
ENST00000635109.1:c.*1586A=	ENSP00000489457.1:n.*1586A=
ENST00000635534.1:c.1780A=	ENSP00000489229.1:p.Asn594=
ENST00000635638.1:c.1792A=	ENSP00000489073.1:p.Asn598=
ENST00000703612.1:c.1780A=	ENSP00000515396.1:p.Asn594=
ENST00000703613.1:c.1840A=	ENSP00000515397.1:p.Asn614=
ENST00000703614.1:c.1789A=	ENSP00000515398.1:p.Asn597=
ENST00000703616.1:c.1915A=	ENSP00000515400.1:p.Asn639=
ENST00000703617.1:c.1234A=	ENSP00000515401.1:p.Asn412=
ENST00000703618.1:c.686A=
XM_011516706.1:c.1933A=	XP_011515008.1:p.Asn645=
XM_017012801.2:c.1864A=	XP_016868290.1:p.Asn622=