Canonical Allele Identifier: CA368965694

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299712A>C (hg19) ; chr7:g.114659657A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659657A>C , CM000669.2:g.114659657A>C	GRCh38
NC_000007.13:g.114299712A>C , CM000669.1:g.114299712A>C	GRCh37
NC_000007.12:g.114086948A>C	NCBI36
NG_007491.2:g.578348A>C
NG_007491.3:g.578348A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1682A>C	ENSP00000385069.4:p.Asn561Thr
ENST00000703612.1:c.1622A>C	ENSP00000515396.1:p.Asn541Thr
ENST00000703613.1:c.1682A>C	ENSP00000515397.1:p.Asn561Thr
ENST00000703614.1:c.1631A>C	ENSP00000515398.1:p.Asn544Thr
ENST00000703616.1:c.1757A>C	ENSP00000515400.1:p.Asn586Thr
ENST00000703617.1:c.1076A>C	ENSP00000515401.1:p.Asn359Thr
ENST00000703618.1:c.545-2408A>C
ENST00000350908.9:c.1631A>C MANE Select	ENSP00000265436.7:p.Asn544Thr
ENST00000393489.8:c.*1425A>C	ENSP00000377129.4:n.*1425A>C
ENST00000350908.8:c.1631A>C	ENSP00000265436.7:p.Asn544Thr
ENST00000393489.7:c.1355A>C	ENSP00000377129.3:p.Asn452Thr
ENST00000393491.7:c.1076A>C	ENSP00000377130.3:p.Asn359Thr
ENST00000393494.6:c.1631A>C	ENSP00000377132.2:p.Asn544Thr
ENST00000393498.6:c.1568A>C	ENSP00000377135.2:p.Asn523Thr
ENST00000403559.8:c.1682A>C	ENSP00000385069.4:p.Asn561Thr
ENST00000408937.7:c.1706A>C	ENSP00000386200.3:p.Asn569Thr
ENST00000412402.5:c.*1349A>C	ENSP00000405470.1:n.*1349A>C
ENST00000441290.6:c.*1631A>C	ENSP00000416825.1:n.*1631A>C
ENST00000634411.1:c.1580A>C	ENSP00000489135.1:p.Asn527Thr
ENST00000634623.1:c.1571A>C	ENSP00000488944.1:p.Asn524Thr
ENST00000635109.1:c.*1428A>C	ENSP00000489457.1:n.*1428A>C
ENST00000635534.1:c.1622A>C	ENSP00000489229.1:p.Asn541Thr
ENST00000635638.1:c.1634A>C	ENSP00000489073.1:p.Asn545Thr
NM_001172766.2:c.1628A>C	NP_001166237.1:p.Asn543Thr
NM_014491.3:c.1631A>C	NP_055306.1:p.Asn544Thr
NM_148898.3:c.1706A>C	NP_683696.2:p.Asn569Thr
NM_148900.3:c.1682A>C	NP_683698.2:p.Asn561Thr
NR_033766.1:n.2016A>C
NR_033767.1:n.2063A>C
XM_011516706.1:c.1775A>C	XP_011515008.1:p.Asn592Thr
XM_017012801.2:c.1706A>C	XP_016868290.1:p.Asn569Thr
NM_014491.4:c.1631A>C MANE Select	NP_055306.1:p.Asn544Thr
NM_001172766.3:c.1628A>C	NP_001166237.1:p.Asn543Thr
NM_148898.4:c.1706A>C	NP_683696.2:p.Asn569Thr
NR_033766.2:n.1999A>C
NR_033767.2:n.2245A>C
NM_148900.4:c.1682A>C	NP_683698.2:p.Asn561Thr