Canonical Allele Identifier: CA368965796

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302142G>C (hg19) ; chr7:g.114662087G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662087G>C , CM000669.2:g.114662087G>C	GRCh38
NC_000007.13:g.114302142G>C , CM000669.1:g.114302142G>C	GRCh37
NC_000007.12:g.114089378G>C	NCBI36
NG_007491.2:g.580778G>C
NG_007491.3:g.580778G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1721G>C	ENSP00000385069.4:p.Ser574Thr
ENST00000703612.1:c.1661G>C	ENSP00000515396.1:p.Ser554Thr
ENST00000703613.1:c.1721G>C	ENSP00000515397.1:p.Ser574Thr
ENST00000703614.1:c.1670G>C	ENSP00000515398.1:p.Ser557Thr
ENST00000703616.1:c.1796G>C	ENSP00000515400.1:p.Ser599Thr
ENST00000703617.1:c.1115G>C	ENSP00000515401.1:p.Ser372Thr
ENST00000703618.1:c.567G>C
ENST00000350908.9:c.1670G>C MANE Select	ENSP00000265436.7:p.Ser557Thr
ENST00000393489.8:c.*1464G>C	ENSP00000377129.4:n.*1464G>C
ENST00000350908.8:c.1670G>C	ENSP00000265436.7:p.Ser557Thr
ENST00000393489.7:c.1394G>C	ENSP00000377129.3:p.Ser465Thr
ENST00000393491.7:c.1115G>C	ENSP00000377130.3:p.Ser372Thr
ENST00000393494.6:c.1670G>C	ENSP00000377132.2:p.Ser557Thr
ENST00000393498.6:c.1607G>C	ENSP00000377135.2:p.Ser536Thr
ENST00000403559.8:c.1721G>C	ENSP00000385069.4:p.Ser574Thr
ENST00000408937.7:c.1745G>C	ENSP00000386200.3:p.Ser582Thr
ENST00000412402.5:c.*1388G>C	ENSP00000405470.1:n.*1388G>C
ENST00000441290.6:c.*1670G>C	ENSP00000416825.1:n.*1670G>C
ENST00000634411.1:c.1619G>C	ENSP00000489135.1:p.Ser540Thr
ENST00000634623.1:c.1610G>C	ENSP00000488944.1:p.Ser537Thr
ENST00000634664.1:n.145G>C
ENST00000635109.1:c.*1467G>C	ENSP00000489457.1:n.*1467G>C
ENST00000635534.1:c.1661G>C	ENSP00000489229.1:p.Ser554Thr
ENST00000635638.1:c.1673G>C	ENSP00000489073.1:p.Ser558Thr
NM_001172766.2:c.1667G>C	NP_001166237.1:p.Ser556Thr
NM_014491.3:c.1670G>C	NP_055306.1:p.Ser557Thr
NM_148898.3:c.1745G>C	NP_683696.2:p.Ser582Thr
NM_148900.3:c.1721G>C	NP_683698.2:p.Ser574Thr
NR_033766.1:n.2055G>C
NR_033767.1:n.2102G>C
XM_011516706.1:c.1814G>C	XP_011515008.1:p.Ser605Thr
XM_017012801.2:c.1745G>C	XP_016868290.1:p.Ser582Thr
NM_014491.4:c.1670G>C MANE Select	NP_055306.1:p.Ser557Thr
NM_001172766.3:c.1667G>C	NP_001166237.1:p.Ser556Thr
NM_148898.4:c.1745G>C	NP_683696.2:p.Ser582Thr
NR_033766.2:n.2038G>C
NR_033767.2:n.2284G>C
NM_148900.4:c.1721G>C	NP_683698.2:p.Ser574Thr