Canonical Allele Identifier: CA457220100

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299665T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659610T>C , CM000669.2:g.114659610T>C	GRCh38
NC_000007.13:g.114299665T>C , CM000669.1:g.114299665T>C	GRCh37
NC_000007.12:g.114086901T>C	NCBI36
NG_007491.2:g.578301T>C
NG_007491.3:g.578301T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1635T>C	ENSP00000385069.4:p.Asn545=
ENST00000703612.1:c.1575T>C	ENSP00000515396.1:p.Asn525=
ENST00000703613.1:c.1635T>C	ENSP00000515397.1:p.Asn545=
ENST00000703614.1:c.1584T>C	ENSP00000515398.1:p.Asn528=
ENST00000703616.1:c.1710T>C	ENSP00000515400.1:p.Asn570=
ENST00000703617.1:c.1029T>C	ENSP00000515401.1:p.Asn343=
ENST00000703618.1:c.545-2455T>C
ENST00000350908.9:c.1584T>C MANE Select	ENSP00000265436.7:p.Asn528=
ENST00000393489.8:c.*1378T>C	ENSP00000377129.4:n.*1378T>C
ENST00000350908.8:c.1584T>C	ENSP00000265436.7:p.Asn528=
ENST00000393489.7:c.1308T>C	ENSP00000377129.3:p.Asn436=
ENST00000393491.7:c.1029T>C	ENSP00000377130.3:p.Asn343=
ENST00000393494.6:c.1584T>C	ENSP00000377132.2:p.Asn528=
ENST00000393498.6:c.1521T>C	ENSP00000377135.2:p.Asn507=
ENST00000403559.8:c.1635T>C	ENSP00000385069.4:p.Asn545=
ENST00000408937.7:c.1659T>C	ENSP00000386200.3:p.Asn553=
ENST00000412402.5:c.*1302T>C	ENSP00000405470.1:n.*1302T>C
ENST00000441290.6:c.*1584T>C	ENSP00000416825.1:n.*1584T>C
ENST00000634411.1:c.1533T>C	ENSP00000489135.1:p.Asn511=
ENST00000634623.1:c.1524T>C	ENSP00000488944.1:p.Asn508=
ENST00000635109.1:c.*1381T>C	ENSP00000489457.1:n.*1381T>C
ENST00000635534.1:c.1575T>C	ENSP00000489229.1:p.Asn525=
ENST00000635638.1:c.1587T>C	ENSP00000489073.1:p.Asn529=
NM_001172766.2:c.1581T>C	NP_001166237.1:p.Asn527=
NM_014491.3:c.1584T>C	NP_055306.1:p.Asn528=
NM_148898.3:c.1659T>C	NP_683696.2:p.Asn553=
NM_148900.3:c.1635T>C	NP_683698.2:p.Asn545=
NR_033766.1:n.1969T>C
NR_033767.1:n.2016T>C
XM_011516706.1:c.1728T>C	XP_011515008.1:p.Asn576=
XM_017012801.2:c.1659T>C	XP_016868290.1:p.Asn553=
NM_014491.4:c.1584T>C MANE Select	NP_055306.1:p.Asn528=
NM_001172766.3:c.1581T>C	NP_001166237.1:p.Asn527=
NM_148898.4:c.1659T>C	NP_683696.2:p.Asn553=
NR_033766.2:n.1952T>C
NR_033767.2:n.2198T>C
NM_148900.4:c.1635T>C	NP_683698.2:p.Asn545=