Canonical Allele Identifier: CA368965777

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302134T>G (hg19) ; chr7:g.114662079T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662079T>G , CM000669.2:g.114662079T>G	GRCh38
NC_000007.13:g.114302134T>G , CM000669.1:g.114302134T>G	GRCh37
NC_000007.12:g.114089370T>G	NCBI36
NG_007491.2:g.580770T>G
NG_007491.3:g.580770T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1713T>G	ENSP00000385069.4:p.His571Gln
ENST00000703612.1:c.1653T>G	ENSP00000515396.1:p.His551Gln
ENST00000703613.1:c.1713T>G	ENSP00000515397.1:p.His571Gln
ENST00000703614.1:c.1662T>G	ENSP00000515398.1:p.His554Gln
ENST00000703616.1:c.1788T>G	ENSP00000515400.1:p.His596Gln
ENST00000703617.1:c.1107T>G	ENSP00000515401.1:p.His369Gln
ENST00000703618.1:c.559T>G
ENST00000350908.9:c.1662T>G MANE Select	ENSP00000265436.7:p.His554Gln
ENST00000393489.8:c.*1456T>G	ENSP00000377129.4:n.*1456T>G
ENST00000350908.8:c.1662T>G	ENSP00000265436.7:p.His554Gln
ENST00000393489.7:c.1386T>G	ENSP00000377129.3:p.His462Gln
ENST00000393491.7:c.1107T>G	ENSP00000377130.3:p.His369Gln
ENST00000393494.6:c.1662T>G	ENSP00000377132.2:p.His554Gln
ENST00000393498.6:c.1599T>G	ENSP00000377135.2:p.His533Gln
ENST00000403559.8:c.1713T>G	ENSP00000385069.4:p.His571Gln
ENST00000408937.7:c.1737T>G	ENSP00000386200.3:p.His579Gln
ENST00000412402.5:c.*1380T>G	ENSP00000405470.1:n.*1380T>G
ENST00000441290.6:c.*1662T>G	ENSP00000416825.1:n.*1662T>G
ENST00000634411.1:c.1611T>G	ENSP00000489135.1:p.His537Gln
ENST00000634623.1:c.1602T>G	ENSP00000488944.1:p.His534Gln
ENST00000634664.1:n.137T>G
ENST00000635109.1:c.*1459T>G	ENSP00000489457.1:n.*1459T>G
ENST00000635534.1:c.1653T>G	ENSP00000489229.1:p.His551Gln
ENST00000635638.1:c.1665T>G	ENSP00000489073.1:p.His555Gln
NM_001172766.2:c.1659T>G	NP_001166237.1:p.His553Gln
NM_014491.3:c.1662T>G	NP_055306.1:p.His554Gln
NM_148898.3:c.1737T>G	NP_683696.2:p.His579Gln
NM_148900.3:c.1713T>G	NP_683698.2:p.His571Gln
NR_033766.1:n.2047T>G
NR_033767.1:n.2094T>G
XM_011516706.1:c.1806T>G	XP_011515008.1:p.His602Gln
XM_017012801.2:c.1737T>G	XP_016868290.1:p.His579Gln
NM_014491.4:c.1662T>G MANE Select	NP_055306.1:p.His554Gln
NM_001172766.3:c.1659T>G	NP_001166237.1:p.His553Gln
NM_148898.4:c.1737T>G	NP_683696.2:p.His579Gln
NR_033766.2:n.2030T>G
NR_033767.2:n.2276T>G
NM_148900.4:c.1713T>G	NP_683698.2:p.His571Gln