Canonical Allele Identifier: CA368965733

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299728G>T (hg19) ; chr7:g.114659673G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659673G>T , CM000669.2:g.114659673G>T	GRCh38
NC_000007.13:g.114299728G>T , CM000669.1:g.114299728G>T	GRCh37
NC_000007.12:g.114086964G>T	NCBI36
NG_007491.2:g.578364G>T
NG_007491.3:g.578364G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1698G>T	ENSP00000385069.4:p.Lys566Asn
ENST00000703612.1:c.1638G>T	ENSP00000515396.1:p.Lys546Asn
ENST00000703613.1:c.1698G>T	ENSP00000515397.1:p.Lys566Asn
ENST00000703614.1:c.1647G>T	ENSP00000515398.1:p.Lys549Asn
ENST00000703616.1:c.1773G>T	ENSP00000515400.1:p.Lys591Asn
ENST00000703617.1:c.1092G>T	ENSP00000515401.1:p.Lys364Asn
ENST00000703618.1:c.545-2392G>T
ENST00000350908.9:c.1647G>T MANE Select	ENSP00000265436.7:p.Lys549Asn
ENST00000393489.8:c.*1441G>T	ENSP00000377129.4:n.*1441G>T
ENST00000350908.8:c.1647G>T	ENSP00000265436.7:p.Lys549Asn
ENST00000393489.7:c.1371G>T	ENSP00000377129.3:p.Lys457Asn
ENST00000393491.7:c.1092G>T	ENSP00000377130.3:p.Lys364Asn
ENST00000393494.6:c.1647G>T	ENSP00000377132.2:p.Lys549Asn
ENST00000393498.6:c.1584G>T	ENSP00000377135.2:p.Lys528Asn
ENST00000403559.8:c.1698G>T	ENSP00000385069.4:p.Lys566Asn
ENST00000408937.7:c.1722G>T	ENSP00000386200.3:p.Lys574Asn
ENST00000412402.5:c.*1365G>T	ENSP00000405470.1:n.*1365G>T
ENST00000441290.6:c.*1647G>T	ENSP00000416825.1:n.*1647G>T
ENST00000634411.1:c.1596G>T	ENSP00000489135.1:p.Lys532Asn
ENST00000634623.1:c.1587G>T	ENSP00000488944.1:p.Lys529Asn
ENST00000635109.1:c.*1444G>T	ENSP00000489457.1:n.*1444G>T
ENST00000635534.1:c.1638G>T	ENSP00000489229.1:p.Lys546Asn
ENST00000635638.1:c.1650G>T	ENSP00000489073.1:p.Lys550Asn
NM_001172766.2:c.1644G>T	NP_001166237.1:p.Lys548Asn
NM_014491.3:c.1647G>T	NP_055306.1:p.Lys549Asn
NM_148898.3:c.1722G>T	NP_683696.2:p.Lys574Asn
NM_148900.3:c.1698G>T	NP_683698.2:p.Lys566Asn
NR_033766.1:n.2032G>T
NR_033767.1:n.2079G>T
XM_011516706.1:c.1791G>T	XP_011515008.1:p.Lys597Asn
XM_017012801.2:c.1722G>T	XP_016868290.1:p.Lys574Asn
NM_014491.4:c.1647G>T MANE Select	NP_055306.1:p.Lys549Asn
NM_001172766.3:c.1644G>T	NP_001166237.1:p.Lys548Asn
NM_148898.4:c.1722G>T	NP_683696.2:p.Lys574Asn
NR_033766.2:n.2015G>T
NR_033767.2:n.2261G>T
NM_148900.4:c.1698G>T	NP_683698.2:p.Lys566Asn