Canonical Allele Identifier: CA457220266

Gene: FOXP2

Linked Data

• dbSNP Id: rs1424508925
• gnomAD v2: 7-114302197-G-A
• gnomAD v3: 7-114662142-G-A
• gnomAD v4: 7-114662142-G-A
• MyVariant Identifiers: chr7:g.114302197G>A (hg19) ; chr7:g.114662142G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662142G>A , CM000669.2:g.114662142G>A	GRCh38
NC_000007.13:g.114302197G>A , CM000669.1:g.114302197G>A	GRCh37
NC_000007.12:g.114089433G>A	NCBI36
NG_007491.2:g.580833G>A
NG_007491.3:g.580833G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1776G>A	ENSP00000385069.4:p.Val592=
ENST00000703612.1:c.1716G>A	ENSP00000515396.1:p.Val572=
ENST00000703613.1:c.1776G>A	ENSP00000515397.1:p.Val592=
ENST00000703614.1:c.1725G>A	ENSP00000515398.1:p.Val575=
ENST00000703616.1:c.1851G>A	ENSP00000515400.1:p.Val617=
ENST00000703617.1:c.1170G>A	ENSP00000515401.1:p.Val390=
ENST00000703618.1:c.622G>A
ENST00000350908.9:c.1725G>A MANE Select	ENSP00000265436.7:p.Val575=
ENST00000393489.8:c.*1519G>A	ENSP00000377129.4:n.*1519G>A
ENST00000350908.8:c.1725G>A	ENSP00000265436.7:p.Val575=
ENST00000393489.7:c.1449G>A	ENSP00000377129.3:p.Val483=
ENST00000393491.7:c.1170G>A	ENSP00000377130.3:p.Val390=
ENST00000393494.6:c.1725G>A	ENSP00000377132.2:p.Val575=
ENST00000393498.6:c.1662G>A	ENSP00000377135.2:p.Val554=
ENST00000403559.8:c.1776G>A	ENSP00000385069.4:p.Val592=
ENST00000408937.7:c.1800G>A	ENSP00000386200.3:p.Val600=
ENST00000412402.5:c.*1443G>A	ENSP00000405470.1:n.*1443G>A
ENST00000441290.6:c.*1725G>A	ENSP00000416825.1:n.*1725G>A
ENST00000634411.1:c.1674G>A	ENSP00000489135.1:p.Val558=
ENST00000634623.1:c.1665G>A	ENSP00000488944.1:p.Val555=
ENST00000634664.1:n.200G>A
ENST00000635109.1:c.*1522G>A	ENSP00000489457.1:n.*1522G>A
ENST00000635534.1:c.1716G>A	ENSP00000489229.1:p.Val572=
ENST00000635638.1:c.1728G>A	ENSP00000489073.1:p.Val576=
NM_001172766.2:c.1722G>A	NP_001166237.1:p.Val574=
NM_014491.3:c.1725G>A	NP_055306.1:p.Val575=
NM_148898.3:c.1800G>A	NP_683696.2:p.Val600=
NM_148900.3:c.1776G>A	NP_683698.2:p.Val592=
NR_033766.1:n.2110G>A
NR_033767.1:n.2157G>A
XM_011516706.1:c.1869G>A	XP_011515008.1:p.Val623=
XM_017012801.2:c.1800G>A	XP_016868290.1:p.Val600=
NM_014491.4:c.1725G>A MANE Select	NP_055306.1:p.Val575=
NM_001172766.3:c.1722G>A	NP_001166237.1:p.Val574=
NM_148898.4:c.1800G>A	NP_683696.2:p.Val600=
NR_033766.2:n.2093G>A
NR_033767.2:n.2339G>A
NM_148900.4:c.1776G>A	NP_683698.2:p.Val592=