Canonical Allele Identifier: CA368965799

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302143C>G (hg19) ; chr7:g.114662088C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662088C>G , CM000669.2:g.114662088C>G	GRCh38
NC_000007.13:g.114302143C>G , CM000669.1:g.114302143C>G	GRCh37
NC_000007.12:g.114089379C>G	NCBI36
NG_007491.2:g.580779C>G
NG_007491.3:g.580779C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1722C>G	ENSP00000385069.4:p.Ser574Arg
ENST00000703612.1:c.1662C>G	ENSP00000515396.1:p.Ser554Arg
ENST00000703613.1:c.1722C>G	ENSP00000515397.1:p.Ser574Arg
ENST00000703614.1:c.1671C>G	ENSP00000515398.1:p.Ser557Arg
ENST00000703616.1:c.1797C>G	ENSP00000515400.1:p.Ser599Arg
ENST00000703617.1:c.1116C>G	ENSP00000515401.1:p.Ser372Arg
ENST00000703618.1:c.568C>G
ENST00000350908.9:c.1671C>G MANE Select	ENSP00000265436.7:p.Ser557Arg
ENST00000393489.8:c.*1465C>G	ENSP00000377129.4:n.*1465C>G
ENST00000350908.8:c.1671C>G	ENSP00000265436.7:p.Ser557Arg
ENST00000393489.7:c.1395C>G	ENSP00000377129.3:p.Ser465Arg
ENST00000393491.7:c.1116C>G	ENSP00000377130.3:p.Ser372Arg
ENST00000393494.6:c.1671C>G	ENSP00000377132.2:p.Ser557Arg
ENST00000393498.6:c.1608C>G	ENSP00000377135.2:p.Ser536Arg
ENST00000403559.8:c.1722C>G	ENSP00000385069.4:p.Ser574Arg
ENST00000408937.7:c.1746C>G	ENSP00000386200.3:p.Ser582Arg
ENST00000412402.5:c.*1389C>G	ENSP00000405470.1:n.*1389C>G
ENST00000441290.6:c.*1671C>G	ENSP00000416825.1:n.*1671C>G
ENST00000634411.1:c.1620C>G	ENSP00000489135.1:p.Ser540Arg
ENST00000634623.1:c.1611C>G	ENSP00000488944.1:p.Ser537Arg
ENST00000634664.1:n.146C>G
ENST00000635109.1:c.*1468C>G	ENSP00000489457.1:n.*1468C>G
ENST00000635534.1:c.1662C>G	ENSP00000489229.1:p.Ser554Arg
ENST00000635638.1:c.1674C>G	ENSP00000489073.1:p.Ser558Arg
NM_001172766.2:c.1668C>G	NP_001166237.1:p.Ser556Arg
NM_014491.3:c.1671C>G	NP_055306.1:p.Ser557Arg
NM_148898.3:c.1746C>G	NP_683696.2:p.Ser582Arg
NM_148900.3:c.1722C>G	NP_683698.2:p.Ser574Arg
NR_033766.1:n.2056C>G
NR_033767.1:n.2103C>G
XM_011516706.1:c.1815C>G	XP_011515008.1:p.Ser605Arg
XM_017012801.2:c.1746C>G	XP_016868290.1:p.Ser582Arg
NM_014491.4:c.1671C>G MANE Select	NP_055306.1:p.Ser557Arg
NM_001172766.3:c.1668C>G	NP_001166237.1:p.Ser556Arg
NM_148898.4:c.1746C>G	NP_683696.2:p.Ser582Arg
NR_033766.2:n.2039C>G
NR_033767.2:n.2285C>G
NM_148900.4:c.1722C>G	NP_683698.2:p.Ser574Arg