Canonical Allele Identifier: CA368965689

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299709G>C (hg19) ; chr7:g.114659654G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659654G>C , CM000669.2:g.114659654G>C	GRCh38
NC_000007.13:g.114299709G>C , CM000669.1:g.114299709G>C	GRCh37
NC_000007.12:g.114086945G>C	NCBI36
NG_007491.2:g.578345G>C
NG_007491.3:g.578345G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1679G>C	ENSP00000385069.4:p.Arg560Pro
ENST00000703612.1:c.1619G>C	ENSP00000515396.1:p.Arg540Pro
ENST00000703613.1:c.1679G>C	ENSP00000515397.1:p.Arg560Pro
ENST00000703614.1:c.1628G>C	ENSP00000515398.1:p.Arg543Pro
ENST00000703616.1:c.1754G>C	ENSP00000515400.1:p.Arg585Pro
ENST00000703617.1:c.1073G>C	ENSP00000515401.1:p.Arg358Pro
ENST00000703618.1:c.545-2411G>C
ENST00000350908.9:c.1628G>C MANE Select	ENSP00000265436.7:p.Arg543Pro
ENST00000393489.8:c.*1422G>C	ENSP00000377129.4:n.*1422G>C
ENST00000350908.8:c.1628G>C	ENSP00000265436.7:p.Arg543Pro
ENST00000393489.7:c.1352G>C	ENSP00000377129.3:p.Arg451Pro
ENST00000393491.7:c.1073G>C	ENSP00000377130.3:p.Arg358Pro
ENST00000393494.6:c.1628G>C	ENSP00000377132.2:p.Arg543Pro
ENST00000393498.6:c.1565G>C	ENSP00000377135.2:p.Arg522Pro
ENST00000403559.8:c.1679G>C	ENSP00000385069.4:p.Arg560Pro
ENST00000408937.7:c.1703G>C	ENSP00000386200.3:p.Arg568Pro
ENST00000412402.5:c.*1346G>C	ENSP00000405470.1:n.*1346G>C
ENST00000441290.6:c.*1628G>C	ENSP00000416825.1:n.*1628G>C
ENST00000634411.1:c.1577G>C	ENSP00000489135.1:p.Arg526Pro
ENST00000634623.1:c.1568G>C	ENSP00000488944.1:p.Arg523Pro
ENST00000635109.1:c.*1425G>C	ENSP00000489457.1:n.*1425G>C
ENST00000635534.1:c.1619G>C	ENSP00000489229.1:p.Arg540Pro
ENST00000635638.1:c.1631G>C	ENSP00000489073.1:p.Arg544Pro
NM_001172766.2:c.1625G>C	NP_001166237.1:p.Arg542Pro
NM_014491.3:c.1628G>C	NP_055306.1:p.Arg543Pro
NM_148898.3:c.1703G>C	NP_683696.2:p.Arg568Pro
NM_148900.3:c.1679G>C	NP_683698.2:p.Arg560Pro
NR_033766.1:n.2013G>C
NR_033767.1:n.2060G>C
XM_011516706.1:c.1772G>C	XP_011515008.1:p.Arg591Pro
XM_017012801.2:c.1703G>C	XP_016868290.1:p.Arg568Pro
NM_014491.4:c.1628G>C MANE Select	NP_055306.1:p.Arg543Pro
NM_001172766.3:c.1625G>C	NP_001166237.1:p.Arg542Pro
NM_148898.4:c.1703G>C	NP_683696.2:p.Arg568Pro
NR_033766.2:n.1996G>C
NR_033767.2:n.2242G>C
NM_148900.4:c.1679G>C	NP_683698.2:p.Arg560Pro