Canonical Allele Identifier: CA368965945

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302207G>C (hg19) ; chr7:g.114662152G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662152G>C , CM000669.2:g.114662152G>C	GRCh38
NC_000007.13:g.114302207G>C , CM000669.1:g.114302207G>C	GRCh37
NC_000007.12:g.114089443G>C	NCBI36
NG_007491.2:g.580843G>C
NG_007491.3:g.580843G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1786G>C	ENSP00000385069.4:p.Glu596Gln
ENST00000703612.1:c.1726G>C	ENSP00000515396.1:p.Glu576Gln
ENST00000703613.1:c.1786G>C	ENSP00000515397.1:p.Glu596Gln
ENST00000703614.1:c.1735G>C	ENSP00000515398.1:p.Glu579Gln
ENST00000703616.1:c.1861G>C	ENSP00000515400.1:p.Glu621Gln
ENST00000703617.1:c.1180G>C	ENSP00000515401.1:p.Glu394Gln
ENST00000703618.1:c.632G>C
ENST00000350908.9:c.1735G>C MANE Select	ENSP00000265436.7:p.Glu579Gln
ENST00000393489.8:c.*1529G>C	ENSP00000377129.4:n.*1529G>C
ENST00000350908.8:c.1735G>C	ENSP00000265436.7:p.Glu579Gln
ENST00000393489.7:c.1459G>C	ENSP00000377129.3:p.Glu487Gln
ENST00000393491.7:c.1180G>C	ENSP00000377130.3:p.Glu394Gln
ENST00000393494.6:c.1735G>C	ENSP00000377132.2:p.Glu579Gln
ENST00000393498.6:c.1672G>C	ENSP00000377135.2:p.Glu558Gln
ENST00000403559.8:c.1786G>C	ENSP00000385069.4:p.Glu596Gln
ENST00000408937.7:c.1810G>C	ENSP00000386200.3:p.Glu604Gln
ENST00000412402.5:c.*1453G>C	ENSP00000405470.1:n.*1453G>C
ENST00000441290.6:c.*1735G>C	ENSP00000416825.1:n.*1735G>C
ENST00000634411.1:c.1684G>C	ENSP00000489135.1:p.Glu562Gln
ENST00000634623.1:c.1675G>C	ENSP00000488944.1:p.Glu559Gln
ENST00000634664.1:n.210G>C
ENST00000635109.1:c.*1532G>C	ENSP00000489457.1:n.*1532G>C
ENST00000635534.1:c.1726G>C	ENSP00000489229.1:p.Glu576Gln
ENST00000635638.1:c.1738G>C	ENSP00000489073.1:p.Glu580Gln
NM_001172766.2:c.1732G>C	NP_001166237.1:p.Glu578Gln
NM_014491.3:c.1735G>C	NP_055306.1:p.Glu579Gln
NM_148898.3:c.1810G>C	NP_683696.2:p.Glu604Gln
NM_148900.3:c.1786G>C	NP_683698.2:p.Glu596Gln
NR_033766.1:n.2120G>C
NR_033767.1:n.2167G>C
XM_011516706.1:c.1879G>C	XP_011515008.1:p.Glu627Gln
XM_017012801.2:c.1810G>C	XP_016868290.1:p.Glu604Gln
NM_014491.4:c.1735G>C MANE Select	NP_055306.1:p.Glu579Gln
NM_001172766.3:c.1732G>C	NP_001166237.1:p.Glu578Gln
NM_148898.4:c.1810G>C	NP_683696.2:p.Glu604Gln
NR_033766.2:n.2103G>C
NR_033767.2:n.2349G>C
NM_148900.4:c.1786G>C	NP_683698.2:p.Glu596Gln