Canonical Allele Identifier: CA368965790

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302139T>C (hg19) ; chr7:g.114662084T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662084T>C , CM000669.2:g.114662084T>C	GRCh38
NC_000007.13:g.114302139T>C , CM000669.1:g.114302139T>C	GRCh37
NC_000007.12:g.114089375T>C	NCBI36
NG_007491.2:g.580775T>C
NG_007491.3:g.580775T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1718T>C	ENSP00000385069.4:p.Leu573Pro
ENST00000703612.1:c.1658T>C	ENSP00000515396.1:p.Leu553Pro
ENST00000703613.1:c.1718T>C	ENSP00000515397.1:p.Leu573Pro
ENST00000703614.1:c.1667T>C	ENSP00000515398.1:p.Leu556Pro
ENST00000703616.1:c.1793T>C	ENSP00000515400.1:p.Leu598Pro
ENST00000703617.1:c.1112T>C	ENSP00000515401.1:p.Leu371Pro
ENST00000703618.1:c.564T>C
ENST00000350908.9:c.1667T>C MANE Select	ENSP00000265436.7:p.Leu556Pro
ENST00000393489.8:c.*1461T>C	ENSP00000377129.4:n.*1461T>C
ENST00000350908.8:c.1667T>C	ENSP00000265436.7:p.Leu556Pro
ENST00000393489.7:c.1391T>C	ENSP00000377129.3:p.Leu464Pro
ENST00000393491.7:c.1112T>C	ENSP00000377130.3:p.Leu371Pro
ENST00000393494.6:c.1667T>C	ENSP00000377132.2:p.Leu556Pro
ENST00000393498.6:c.1604T>C	ENSP00000377135.2:p.Leu535Pro
ENST00000403559.8:c.1718T>C	ENSP00000385069.4:p.Leu573Pro
ENST00000408937.7:c.1742T>C	ENSP00000386200.3:p.Leu581Pro
ENST00000412402.5:c.*1385T>C	ENSP00000405470.1:n.*1385T>C
ENST00000441290.6:c.*1667T>C	ENSP00000416825.1:n.*1667T>C
ENST00000634411.1:c.1616T>C	ENSP00000489135.1:p.Leu539Pro
ENST00000634623.1:c.1607T>C	ENSP00000488944.1:p.Leu536Pro
ENST00000634664.1:n.142T>C
ENST00000635109.1:c.*1464T>C	ENSP00000489457.1:n.*1464T>C
ENST00000635534.1:c.1658T>C	ENSP00000489229.1:p.Leu553Pro
ENST00000635638.1:c.1670T>C	ENSP00000489073.1:p.Leu557Pro
NM_001172766.2:c.1664T>C	NP_001166237.1:p.Leu555Pro
NM_014491.3:c.1667T>C	NP_055306.1:p.Leu556Pro
NM_148898.3:c.1742T>C	NP_683696.2:p.Leu581Pro
NM_148900.3:c.1718T>C	NP_683698.2:p.Leu573Pro
NR_033766.1:n.2052T>C
NR_033767.1:n.2099T>C
XM_011516706.1:c.1811T>C	XP_011515008.1:p.Leu604Pro
XM_017012801.2:c.1742T>C	XP_016868290.1:p.Leu581Pro
NM_014491.4:c.1667T>C MANE Select	NP_055306.1:p.Leu556Pro
NM_001172766.3:c.1664T>C	NP_001166237.1:p.Leu555Pro
NM_148898.4:c.1742T>C	NP_683696.2:p.Leu581Pro
NR_033766.2:n.2035T>C
NR_033767.2:n.2281T>C
NM_148900.4:c.1718T>C	NP_683698.2:p.Leu573Pro