Canonical Allele Identifier: CA368965948

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302208A>G (hg19) ; chr7:g.114662153A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662153A>G , CM000669.2:g.114662153A>G	GRCh38
NC_000007.13:g.114302208A>G , CM000669.1:g.114302208A>G	GRCh37
NC_000007.12:g.114089444A>G	NCBI36
NG_007491.2:g.580844A>G
NG_007491.3:g.580844A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1787A>G	ENSP00000385069.4:p.Glu596Gly
ENST00000703612.1:c.1727A>G	ENSP00000515396.1:p.Glu576Gly
ENST00000703613.1:c.1787A>G	ENSP00000515397.1:p.Glu596Gly
ENST00000703614.1:c.1736A>G	ENSP00000515398.1:p.Glu579Gly
ENST00000703616.1:c.1862A>G	ENSP00000515400.1:p.Glu621Gly
ENST00000703617.1:c.1181A>G	ENSP00000515401.1:p.Glu394Gly
ENST00000703618.1:c.633A>G
ENST00000350908.9:c.1736A>G MANE Select	ENSP00000265436.7:p.Glu579Gly
ENST00000393489.8:c.*1530A>G	ENSP00000377129.4:n.*1530A>G
ENST00000350908.8:c.1736A>G	ENSP00000265436.7:p.Glu579Gly
ENST00000393489.7:c.1460A>G	ENSP00000377129.3:p.Glu487Gly
ENST00000393491.7:c.1181A>G	ENSP00000377130.3:p.Glu394Gly
ENST00000393494.6:c.1736A>G	ENSP00000377132.2:p.Glu579Gly
ENST00000393498.6:c.1673A>G	ENSP00000377135.2:p.Glu558Gly
ENST00000403559.8:c.1787A>G	ENSP00000385069.4:p.Glu596Gly
ENST00000408937.7:c.1811A>G	ENSP00000386200.3:p.Glu604Gly
ENST00000412402.5:c.*1454A>G	ENSP00000405470.1:n.*1454A>G
ENST00000441290.6:c.*1736A>G	ENSP00000416825.1:n.*1736A>G
ENST00000634411.1:c.1685A>G	ENSP00000489135.1:p.Glu562Gly
ENST00000634623.1:c.1676A>G	ENSP00000488944.1:p.Glu559Gly
ENST00000634664.1:n.211A>G
ENST00000635109.1:c.*1533A>G	ENSP00000489457.1:n.*1533A>G
ENST00000635534.1:c.1727A>G	ENSP00000489229.1:p.Glu576Gly
ENST00000635638.1:c.1739A>G	ENSP00000489073.1:p.Glu580Gly
NM_001172766.2:c.1733A>G	NP_001166237.1:p.Glu578Gly
NM_014491.3:c.1736A>G	NP_055306.1:p.Glu579Gly
NM_148898.3:c.1811A>G	NP_683696.2:p.Glu604Gly
NM_148900.3:c.1787A>G	NP_683698.2:p.Glu596Gly
NR_033766.1:n.2121A>G
NR_033767.1:n.2168A>G
XM_011516706.1:c.1880A>G	XP_011515008.1:p.Glu627Gly
XM_017012801.2:c.1811A>G	XP_016868290.1:p.Glu604Gly
NM_014491.4:c.1736A>G MANE Select	NP_055306.1:p.Glu579Gly
NM_001172766.3:c.1733A>G	NP_001166237.1:p.Glu578Gly
NM_148898.4:c.1811A>G	NP_683696.2:p.Glu604Gly
NR_033766.2:n.2104A>G
NR_033767.2:n.2350A>G
NM_148900.4:c.1787A>G	NP_683698.2:p.Glu596Gly