Canonical Allele Identifier: CA164884181

Gene: FOXP2

Linked Data

• dbSNP Id: rs112732214
• MyVariant Identifiers: chr7:g.114302145T>C (hg19) ; chr7:g.114662090T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662090T>C , CM000669.2:g.114662090T>C	GRCh38
NC_000007.13:g.114302145T>C , CM000669.1:g.114302145T>C	GRCh37
NC_000007.12:g.114089381T>C	NCBI36
NG_007491.2:g.580781T>C
NG_007491.3:g.580781T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1724T>C	ENSP00000385069.4:p.Leu575Pro
ENST00000703612.1:c.1664T>C	ENSP00000515396.1:p.Leu555Pro
ENST00000703613.1:c.1724T>C	ENSP00000515397.1:p.Leu575Pro
ENST00000703614.1:c.1673T>C	ENSP00000515398.1:p.Leu558Pro
ENST00000703616.1:c.1799T>C	ENSP00000515400.1:p.Leu600Pro
ENST00000703617.1:c.1118T>C	ENSP00000515401.1:p.Leu373Pro
ENST00000703618.1:c.570T>C
ENST00000350908.9:c.1673T>C MANE Select	ENSP00000265436.7:p.Leu558Pro
ENST00000393489.8:c.*1467T>C	ENSP00000377129.4:n.*1467T>C
ENST00000350908.8:c.1673T>C	ENSP00000265436.7:p.Leu558Pro
ENST00000393489.7:c.1397T>C	ENSP00000377129.3:p.Leu466Pro
ENST00000393491.7:c.1118T>C	ENSP00000377130.3:p.Leu373Pro
ENST00000393494.6:c.1673T>C	ENSP00000377132.2:p.Leu558Pro
ENST00000393498.6:c.1610T>C	ENSP00000377135.2:p.Leu537Pro
ENST00000403559.8:c.1724T>C	ENSP00000385069.4:p.Leu575Pro
ENST00000408937.7:c.1748T>C	ENSP00000386200.3:p.Leu583Pro
ENST00000412402.5:c.*1391T>C	ENSP00000405470.1:n.*1391T>C
ENST00000441290.6:c.*1673T>C	ENSP00000416825.1:n.*1673T>C
ENST00000634411.1:c.1622T>C	ENSP00000489135.1:p.Leu541Pro
ENST00000634623.1:c.1613T>C	ENSP00000488944.1:p.Leu538Pro
ENST00000634664.1:n.148T>C
ENST00000635109.1:c.*1470T>C	ENSP00000489457.1:n.*1470T>C
ENST00000635534.1:c.1664T>C	ENSP00000489229.1:p.Leu555Pro
ENST00000635638.1:c.1676T>C	ENSP00000489073.1:p.Leu559Pro
NM_001172766.2:c.1670T>C	NP_001166237.1:p.Leu557Pro
NM_014491.3:c.1673T>C	NP_055306.1:p.Leu558Pro
NM_148898.3:c.1748T>C	NP_683696.2:p.Leu583Pro
NM_148900.3:c.1724T>C	NP_683698.2:p.Leu575Pro
NR_033766.1:n.2058T>C
NR_033767.1:n.2105T>C
XM_011516706.1:c.1817T>C	XP_011515008.1:p.Leu606Pro
XM_017012801.2:c.1748T>C	XP_016868290.1:p.Leu583Pro
NM_014491.4:c.1673T>C MANE Select	NP_055306.1:p.Leu558Pro
NM_001172766.3:c.1670T>C	NP_001166237.1:p.Leu557Pro
NM_148898.4:c.1748T>C	NP_683696.2:p.Leu583Pro
NR_033766.2:n.2041T>C
NR_033767.2:n.2287T>C
NM_148900.4:c.1724T>C	NP_683698.2:p.Leu575Pro