Canonical Allele Identifier: CA1736047878

Gene: FOXP2

Linked Data

• dbSNP Id: rs1806906051

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662168_114662169insAAAAAATGGCAAAAATAATATT , CM000669.2:g.114662168_114662169insAAAAAATGGCAAAAATAATATT	GRCh38
NC_000007.13:g.114302223_114302224insAAAAAATGGCAAAAATAATATT , CM000669.1:g.114302223_114302224insAAAAAATGGCAAAAATAATATT	GRCh37
NC_000007.12:g.114089459_114089460insAAAAAATGGCAAAAATAATATT	NCBI36
NG_007491.2:g.580859_580860insAAAAAATGGCAAAAATAATATT
NG_007491.3:g.580859_580860insAAAAAATGGCAAAAATAATATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1802_1803insAAAAAATGGCAAAAATAATATT	ENSP00000385069.4:p.Ser602LysfsTer32
ENST00000703612.1:c.1742_1743insAAAAAATGGCAAAAATAATATT	ENSP00000515396.1:p.Ser582LysfsTer32
ENST00000703613.1:c.1802_1803insAAAAAATGGCAAAAATAATATT	ENSP00000515397.1:p.Ser602LysfsTer32
ENST00000703614.1:c.1751_1752insAAAAAATGGCAAAAATAATATT	ENSP00000515398.1:p.Ser585LysfsTer32
ENST00000703616.1:c.1877_1878insAAAAAATGGCAAAAATAATATT	ENSP00000515400.1:p.Ser627LysfsTer32
ENST00000703617.1:c.1196_1197insAAAAAATGGCAAAAATAATATT	ENSP00000515401.1:p.Ser400LysfsTer32
ENST00000703618.1:c.648_649insAAAAAATGGCAAAAATAATATT
ENST00000350908.9:c.1751_1752insAAAAAATGGCAAAAATAATATT MANE Select	ENSP00000265436.7:p.Ser585LysfsTer32
ENST00000393489.8:c.*1545_*1546insAAAAAATGGCAAAAATAATATT	ENSP00000377129.4:n.*1545_*1546insAAAAAATGGCAAAAATAATATT
ENST00000350908.8:c.1751_1752insAAAAAATGGCAAAAATAATATT	ENSP00000265436.7:p.Ser585LysfsTer32
ENST00000393489.7:c.1475_1476insAAAAAATGGCAAAAATAATATT	ENSP00000377129.3:p.Ser493LysfsTer32
ENST00000393491.7:c.1196_1197insAAAAAATGGCAAAAATAATATT	ENSP00000377130.3:p.Ser400LysfsTer32
ENST00000393494.6:c.1751_1752insAAAAAATGGCAAAAATAATATT	ENSP00000377132.2:p.Ser585LysfsTer32
ENST00000393498.6:c.1688_1689insAAAAAATGGCAAAAATAATATT	ENSP00000377135.2:p.Ser564LysfsTer32
ENST00000403559.8:c.1802_1803insAAAAAATGGCAAAAATAATATT	ENSP00000385069.4:p.Ser602LysfsTer32
ENST00000408937.7:c.1826_1827insAAAAAATGGCAAAAATAATATT	ENSP00000386200.3:p.Ser610LysfsTer32
ENST00000412402.5:c.*1469_*1470insAAAAAATGGCAAAAATAATATT	ENSP00000405470.1:n.*1469_*1470insAAAAAATGGCAAAAATAATATT
ENST00000441290.6:c.*1751_*1752insAAAAAATGGCAAAAATAATATT	ENSP00000416825.1:n.*1751_*1752insAAAAAATGGCAAAAATAATATT
ENST00000634411.1:c.1700_1701insAAAAAATGGCAAAAATAATATT	ENSP00000489135.1:p.Ser568LysfsTer32
ENST00000634623.1:c.1691_1692insAAAAAATGGCAAAAATAATATT	ENSP00000488944.1:p.Ser565LysfsTer32
ENST00000634664.1:n.226_227insAAAAAATGGCAAAAATAATATT
ENST00000635109.1:c.*1548_*1549insAAAAAATGGCAAAAATAATATT	ENSP00000489457.1:n.*1548_*1549insAAAAAATGGCAAAAATAATATT
ENST00000635534.1:c.1742_1743insAAAAAATGGCAAAAATAATATT	ENSP00000489229.1:p.Ser582LysfsTer32
ENST00000635638.1:c.1754_1755insAAAAAATGGCAAAAATAATATT	ENSP00000489073.1:p.Ser586LysfsTer32
NM_001172766.2:c.1748_1749insAAAAAATGGCAAAAATAATATT	NP_001166237.1:p.Ser584LysfsTer32
NM_014491.3:c.1751_1752insAAAAAATGGCAAAAATAATATT	NP_055306.1:p.Ser585LysfsTer32
NM_148898.3:c.1826_1827insAAAAAATGGCAAAAATAATATT	NP_683696.2:p.Ser610LysfsTer32
NM_148900.3:c.1802_1803insAAAAAATGGCAAAAATAATATT	NP_683698.2:p.Ser602LysfsTer32
NR_033766.1:n.2136_2137insAAAAAATGGCAAAAATAATATT
NR_033767.1:n.2183_2184insAAAAAATGGCAAAAATAATATT
XM_011516706.1:c.1895_1896insAAAAAATGGCAAAAATAATATT	XP_011515008.1:p.Ser633LysfsTer32
XM_017012801.2:c.1826_1827insAAAAAATGGCAAAAATAATATT	XP_016868290.1:p.Ser610LysfsTer32
NM_014491.4:c.1751_1752insAAAAAATGGCAAAAATAATATT MANE Select	NP_055306.1:p.Ser585LysfsTer32
NM_001172766.3:c.1748_1749insAAAAAATGGCAAAAATAATATT	NP_001166237.1:p.Ser584LysfsTer32
NM_148898.4:c.1826_1827insAAAAAATGGCAAAAATAATATT	NP_683696.2:p.Ser610LysfsTer32
NR_033766.2:n.2119_2120insAAAAAATGGCAAAAATAATATT
NR_033767.2:n.2365_2366insAAAAAATGGCAAAAATAATATT
NM_148900.4:c.1802_1803insAAAAAATGGCAAAAATAATATT	NP_683698.2:p.Ser602LysfsTer32