Canonical Allele Identifier: CA457220241

Gene: FOXP2

Linked Data

• dbSNP Id: rs1806903401
• MyVariant Identifiers: chr7:g.114302176T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662121T>C , CM000669.2:g.114662121T>C	GRCh38
NC_000007.13:g.114302176T>C , CM000669.1:g.114302176T>C	GRCh37
NC_000007.12:g.114089412T>C	NCBI36
NG_007491.2:g.580812T>C
NG_007491.3:g.580812T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1755T>C	ENSP00000385069.4:p.Val585=
ENST00000703612.1:c.1695T>C	ENSP00000515396.1:p.Val565=
ENST00000703613.1:c.1755T>C	ENSP00000515397.1:p.Val585=
ENST00000703614.1:c.1704T>C	ENSP00000515398.1:p.Val568=
ENST00000703616.1:c.1830T>C	ENSP00000515400.1:p.Val610=
ENST00000703617.1:c.1149T>C	ENSP00000515401.1:p.Val383=
ENST00000703618.1:c.601T>C
ENST00000350908.9:c.1704T>C MANE Select	ENSP00000265436.7:p.Val568=
ENST00000393489.8:c.*1498T>C	ENSP00000377129.4:n.*1498T>C
ENST00000350908.8:c.1704T>C	ENSP00000265436.7:p.Val568=
ENST00000393489.7:c.1428T>C	ENSP00000377129.3:p.Val476=
ENST00000393491.7:c.1149T>C	ENSP00000377130.3:p.Val383=
ENST00000393494.6:c.1704T>C	ENSP00000377132.2:p.Val568=
ENST00000393498.6:c.1641T>C	ENSP00000377135.2:p.Val547=
ENST00000403559.8:c.1755T>C	ENSP00000385069.4:p.Val585=
ENST00000408937.7:c.1779T>C	ENSP00000386200.3:p.Val593=
ENST00000412402.5:c.*1422T>C	ENSP00000405470.1:n.*1422T>C
ENST00000441290.6:c.*1704T>C	ENSP00000416825.1:n.*1704T>C
ENST00000634411.1:c.1653T>C	ENSP00000489135.1:p.Val551=
ENST00000634623.1:c.1644T>C	ENSP00000488944.1:p.Val548=
ENST00000634664.1:n.179T>C
ENST00000635109.1:c.*1501T>C	ENSP00000489457.1:n.*1501T>C
ENST00000635534.1:c.1695T>C	ENSP00000489229.1:p.Val565=
ENST00000635638.1:c.1707T>C	ENSP00000489073.1:p.Val569=
NM_001172766.2:c.1701T>C	NP_001166237.1:p.Val567=
NM_014491.3:c.1704T>C	NP_055306.1:p.Val568=
NM_148898.3:c.1779T>C	NP_683696.2:p.Val593=
NM_148900.3:c.1755T>C	NP_683698.2:p.Val585=
NR_033766.1:n.2089T>C
NR_033767.1:n.2136T>C
XM_011516706.1:c.1848T>C	XP_011515008.1:p.Val616=
XM_017012801.2:c.1779T>C	XP_016868290.1:p.Val593=
NM_014491.4:c.1704T>C MANE Select	NP_055306.1:p.Val568=
NM_001172766.3:c.1701T>C	NP_001166237.1:p.Val567=
NM_148898.4:c.1779T>C	NP_683696.2:p.Val593=
NR_033766.2:n.2072T>C
NR_033767.2:n.2318T>C
NM_148900.4:c.1755T>C	NP_683698.2:p.Val585=