Canonical Allele Identifier: CA368965778

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302135A>C (hg19) ; chr7:g.114662080A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662080A>C , CM000669.2:g.114662080A>C	GRCh38
NC_000007.13:g.114302135A>C , CM000669.1:g.114302135A>C	GRCh37
NC_000007.12:g.114089371A>C	NCBI36
NG_007491.2:g.580771A>C
NG_007491.3:g.580771A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1714A>C	ENSP00000385069.4:p.Asn572His
ENST00000703612.1:c.1654A>C	ENSP00000515396.1:p.Asn552His
ENST00000703613.1:c.1714A>C	ENSP00000515397.1:p.Asn572His
ENST00000703614.1:c.1663A>C	ENSP00000515398.1:p.Asn555His
ENST00000703616.1:c.1789A>C	ENSP00000515400.1:p.Asn597His
ENST00000703617.1:c.1108A>C	ENSP00000515401.1:p.Asn370His
ENST00000703618.1:c.560A>C
ENST00000350908.9:c.1663A>C MANE Select	ENSP00000265436.7:p.Asn555His
ENST00000393489.8:c.*1457A>C	ENSP00000377129.4:n.*1457A>C
ENST00000350908.8:c.1663A>C	ENSP00000265436.7:p.Asn555His
ENST00000393489.7:c.1387A>C	ENSP00000377129.3:p.Asn463His
ENST00000393491.7:c.1108A>C	ENSP00000377130.3:p.Asn370His
ENST00000393494.6:c.1663A>C	ENSP00000377132.2:p.Asn555His
ENST00000393498.6:c.1600A>C	ENSP00000377135.2:p.Asn534His
ENST00000403559.8:c.1714A>C	ENSP00000385069.4:p.Asn572His
ENST00000408937.7:c.1738A>C	ENSP00000386200.3:p.Asn580His
ENST00000412402.5:c.*1381A>C	ENSP00000405470.1:n.*1381A>C
ENST00000441290.6:c.*1663A>C	ENSP00000416825.1:n.*1663A>C
ENST00000634411.1:c.1612A>C	ENSP00000489135.1:p.Asn538His
ENST00000634623.1:c.1603A>C	ENSP00000488944.1:p.Asn535His
ENST00000634664.1:n.138A>C
ENST00000635109.1:c.*1460A>C	ENSP00000489457.1:n.*1460A>C
ENST00000635534.1:c.1654A>C	ENSP00000489229.1:p.Asn552His
ENST00000635638.1:c.1666A>C	ENSP00000489073.1:p.Asn556His
NM_001172766.2:c.1660A>C	NP_001166237.1:p.Asn554His
NM_014491.3:c.1663A>C	NP_055306.1:p.Asn555His
NM_148898.3:c.1738A>C	NP_683696.2:p.Asn580His
NM_148900.3:c.1714A>C	NP_683698.2:p.Asn572His
NR_033766.1:n.2048A>C
NR_033767.1:n.2095A>C
XM_011516706.1:c.1807A>C	XP_011515008.1:p.Asn603His
XM_017012801.2:c.1738A>C	XP_016868290.1:p.Asn580His
NM_014491.4:c.1663A>C MANE Select	NP_055306.1:p.Asn555His
NM_001172766.3:c.1660A>C	NP_001166237.1:p.Asn554His
NM_148898.4:c.1738A>C	NP_683696.2:p.Asn580His
NR_033766.2:n.2031A>C
NR_033767.2:n.2277A>C
NM_148900.4:c.1714A>C	NP_683698.2:p.Asn572His