Canonical Allele Identifier: CA457220265

Gene: FOXP2

Linked Data

• gnomAD v4: 7-114662139-T-G
• MyVariant Identifiers: chr7:g.114302194T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662139T>G , CM000669.2:g.114662139T>G	GRCh38
NC_000007.13:g.114302194T>G , CM000669.1:g.114302194T>G	GRCh37
NC_000007.12:g.114089430T>G	NCBI36
NG_007491.2:g.580830T>G
NG_007491.3:g.580830T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1773T>G	ENSP00000385069.4:p.Thr591=
ENST00000703612.1:c.1713T>G	ENSP00000515396.1:p.Thr571=
ENST00000703613.1:c.1773T>G	ENSP00000515397.1:p.Thr591=
ENST00000703614.1:c.1722T>G	ENSP00000515398.1:p.Thr574=
ENST00000703616.1:c.1848T>G	ENSP00000515400.1:p.Thr616=
ENST00000703617.1:c.1167T>G	ENSP00000515401.1:p.Thr389=
ENST00000703618.1:c.619T>G
ENST00000350908.9:c.1722T>G MANE Select	ENSP00000265436.7:p.Thr574=
ENST00000393489.8:c.*1516T>G	ENSP00000377129.4:n.*1516T>G
ENST00000350908.8:c.1722T>G	ENSP00000265436.7:p.Thr574=
ENST00000393489.7:c.1446T>G	ENSP00000377129.3:p.Thr482=
ENST00000393491.7:c.1167T>G	ENSP00000377130.3:p.Thr389=
ENST00000393494.6:c.1722T>G	ENSP00000377132.2:p.Thr574=
ENST00000393498.6:c.1659T>G	ENSP00000377135.2:p.Thr553=
ENST00000403559.8:c.1773T>G	ENSP00000385069.4:p.Thr591=
ENST00000408937.7:c.1797T>G	ENSP00000386200.3:p.Thr599=
ENST00000412402.5:c.*1440T>G	ENSP00000405470.1:n.*1440T>G
ENST00000441290.6:c.*1722T>G	ENSP00000416825.1:n.*1722T>G
ENST00000634411.1:c.1671T>G	ENSP00000489135.1:p.Thr557=
ENST00000634623.1:c.1662T>G	ENSP00000488944.1:p.Thr554=
ENST00000634664.1:n.197T>G
ENST00000635109.1:c.*1519T>G	ENSP00000489457.1:n.*1519T>G
ENST00000635534.1:c.1713T>G	ENSP00000489229.1:p.Thr571=
ENST00000635638.1:c.1725T>G	ENSP00000489073.1:p.Thr575=
NM_001172766.2:c.1719T>G	NP_001166237.1:p.Thr573=
NM_014491.3:c.1722T>G	NP_055306.1:p.Thr574=
NM_148898.3:c.1797T>G	NP_683696.2:p.Thr599=
NM_148900.3:c.1773T>G	NP_683698.2:p.Thr591=
NR_033766.1:n.2107T>G
NR_033767.1:n.2154T>G
XM_011516706.1:c.1866T>G	XP_011515008.1:p.Thr622=
XM_017012801.2:c.1797T>G	XP_016868290.1:p.Thr599=
NM_014491.4:c.1722T>G MANE Select	NP_055306.1:p.Thr574=
NM_001172766.3:c.1719T>G	NP_001166237.1:p.Thr573=
NM_148898.4:c.1797T>G	NP_683696.2:p.Thr599=
NR_033766.2:n.2090T>G
NR_033767.2:n.2336T>G
NM_148900.4:c.1773T>G	NP_683698.2:p.Thr591=