Canonical Allele Identifier: CA457220136

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299698T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659643T>C , CM000669.2:g.114659643T>C	GRCh38
NC_000007.13:g.114299698T>C , CM000669.1:g.114299698T>C	GRCh37
NC_000007.12:g.114086934T>C	NCBI36
NG_007491.2:g.578334T>C
NG_007491.3:g.578334T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1668T>C	ENSP00000385069.4:p.Ala556=
ENST00000703612.1:c.1608T>C	ENSP00000515396.1:p.Ala536=
ENST00000703613.1:c.1668T>C	ENSP00000515397.1:p.Ala556=
ENST00000703614.1:c.1617T>C	ENSP00000515398.1:p.Ala539=
ENST00000703616.1:c.1743T>C	ENSP00000515400.1:p.Ala581=
ENST00000703617.1:c.1062T>C	ENSP00000515401.1:p.Ala354=
ENST00000703618.1:c.545-2422T>C
ENST00000350908.9:c.1617T>C MANE Select	ENSP00000265436.7:p.Ala539=
ENST00000393489.8:c.*1411T>C	ENSP00000377129.4:n.*1411T>C
ENST00000350908.8:c.1617T>C	ENSP00000265436.7:p.Ala539=
ENST00000393489.7:c.1341T>C	ENSP00000377129.3:p.Ala447=
ENST00000393491.7:c.1062T>C	ENSP00000377130.3:p.Ala354=
ENST00000393494.6:c.1617T>C	ENSP00000377132.2:p.Ala539=
ENST00000393498.6:c.1554T>C	ENSP00000377135.2:p.Ala518=
ENST00000403559.8:c.1668T>C	ENSP00000385069.4:p.Ala556=
ENST00000408937.7:c.1692T>C	ENSP00000386200.3:p.Ala564=
ENST00000412402.5:c.*1335T>C	ENSP00000405470.1:n.*1335T>C
ENST00000441290.6:c.*1617T>C	ENSP00000416825.1:n.*1617T>C
ENST00000634411.1:c.1566T>C	ENSP00000489135.1:p.Ala522=
ENST00000634623.1:c.1557T>C	ENSP00000488944.1:p.Ala519=
ENST00000635109.1:c.*1414T>C	ENSP00000489457.1:n.*1414T>C
ENST00000635534.1:c.1608T>C	ENSP00000489229.1:p.Ala536=
ENST00000635638.1:c.1620T>C	ENSP00000489073.1:p.Ala540=
NM_001172766.2:c.1614T>C	NP_001166237.1:p.Ala538=
NM_014491.3:c.1617T>C	NP_055306.1:p.Ala539=
NM_148898.3:c.1692T>C	NP_683696.2:p.Ala564=
NM_148900.3:c.1668T>C	NP_683698.2:p.Ala556=
NR_033766.1:n.2002T>C
NR_033767.1:n.2049T>C
XM_011516706.1:c.1761T>C	XP_011515008.1:p.Ala587=
XM_017012801.2:c.1692T>C	XP_016868290.1:p.Ala564=
NM_014491.4:c.1617T>C MANE Select	NP_055306.1:p.Ala539=
NM_001172766.3:c.1614T>C	NP_001166237.1:p.Ala538=
NM_148898.4:c.1692T>C	NP_683696.2:p.Ala564=
NR_033766.2:n.1985T>C
NR_033767.2:n.2231T>C
NM_148900.4:c.1668T>C	NP_683698.2:p.Ala556=