Canonical Allele Identifier: CA368965781

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302136A>C (hg19) ; chr7:g.114662081A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662081A>C , CM000669.2:g.114662081A>C	GRCh38
NC_000007.13:g.114302136A>C , CM000669.1:g.114302136A>C	GRCh37
NC_000007.12:g.114089372A>C	NCBI36
NG_007491.2:g.580772A>C
NG_007491.3:g.580772A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1715A>C	ENSP00000385069.4:p.Asn572Thr
ENST00000703612.1:c.1655A>C	ENSP00000515396.1:p.Asn552Thr
ENST00000703613.1:c.1715A>C	ENSP00000515397.1:p.Asn572Thr
ENST00000703614.1:c.1664A>C	ENSP00000515398.1:p.Asn555Thr
ENST00000703616.1:c.1790A>C	ENSP00000515400.1:p.Asn597Thr
ENST00000703617.1:c.1109A>C	ENSP00000515401.1:p.Asn370Thr
ENST00000703618.1:c.561A>C
ENST00000350908.9:c.1664A>C MANE Select	ENSP00000265436.7:p.Asn555Thr
ENST00000393489.8:c.*1458A>C	ENSP00000377129.4:n.*1458A>C
ENST00000350908.8:c.1664A>C	ENSP00000265436.7:p.Asn555Thr
ENST00000393489.7:c.1388A>C	ENSP00000377129.3:p.Asn463Thr
ENST00000393491.7:c.1109A>C	ENSP00000377130.3:p.Asn370Thr
ENST00000393494.6:c.1664A>C	ENSP00000377132.2:p.Asn555Thr
ENST00000393498.6:c.1601A>C	ENSP00000377135.2:p.Asn534Thr
ENST00000403559.8:c.1715A>C	ENSP00000385069.4:p.Asn572Thr
ENST00000408937.7:c.1739A>C	ENSP00000386200.3:p.Asn580Thr
ENST00000412402.5:c.*1382A>C	ENSP00000405470.1:n.*1382A>C
ENST00000441290.6:c.*1664A>C	ENSP00000416825.1:n.*1664A>C
ENST00000634411.1:c.1613A>C	ENSP00000489135.1:p.Asn538Thr
ENST00000634623.1:c.1604A>C	ENSP00000488944.1:p.Asn535Thr
ENST00000634664.1:n.139A>C
ENST00000635109.1:c.*1461A>C	ENSP00000489457.1:n.*1461A>C
ENST00000635534.1:c.1655A>C	ENSP00000489229.1:p.Asn552Thr
ENST00000635638.1:c.1667A>C	ENSP00000489073.1:p.Asn556Thr
NM_001172766.2:c.1661A>C	NP_001166237.1:p.Asn554Thr
NM_014491.3:c.1664A>C	NP_055306.1:p.Asn555Thr
NM_148898.3:c.1739A>C	NP_683696.2:p.Asn580Thr
NM_148900.3:c.1715A>C	NP_683698.2:p.Asn572Thr
NR_033766.1:n.2049A>C
NR_033767.1:n.2096A>C
XM_011516706.1:c.1808A>C	XP_011515008.1:p.Asn603Thr
XM_017012801.2:c.1739A>C	XP_016868290.1:p.Asn580Thr
NM_014491.4:c.1664A>C MANE Select	NP_055306.1:p.Asn555Thr
NM_001172766.3:c.1661A>C	NP_001166237.1:p.Asn554Thr
NM_148898.4:c.1739A>C	NP_683696.2:p.Asn580Thr
NR_033766.2:n.2032A>C
NR_033767.2:n.2278A>C
NM_148900.4:c.1715A>C	NP_683698.2:p.Asn572Thr