Canonical Allele Identifier: CA368965793

Gene: FOXP2

Linked Data

• COSMIC: COSM4685465 ; COSM4685466
• MyVariant Identifiers: chr7:g.114302141A>G (hg19) ; chr7:g.114662086A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662086A>G , CM000669.2:g.114662086A>G	GRCh38
NC_000007.13:g.114302141A>G , CM000669.1:g.114302141A>G	GRCh37
NC_000007.12:g.114089377A>G	NCBI36
NG_007491.2:g.580777A>G
NG_007491.3:g.580777A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1720A>G	ENSP00000385069.4:p.Ser574Gly
ENST00000703612.1:c.1660A>G	ENSP00000515396.1:p.Ser554Gly
ENST00000703613.1:c.1720A>G	ENSP00000515397.1:p.Ser574Gly
ENST00000703614.1:c.1669A>G	ENSP00000515398.1:p.Ser557Gly
ENST00000703616.1:c.1795A>G	ENSP00000515400.1:p.Ser599Gly
ENST00000703617.1:c.1114A>G	ENSP00000515401.1:p.Ser372Gly
ENST00000703618.1:c.566A>G
ENST00000350908.9:c.1669A>G MANE Select	ENSP00000265436.7:p.Ser557Gly
ENST00000393489.8:c.*1463A>G	ENSP00000377129.4:n.*1463A>G
ENST00000350908.8:c.1669A>G	ENSP00000265436.7:p.Ser557Gly
ENST00000393489.7:c.1393A>G	ENSP00000377129.3:p.Ser465Gly
ENST00000393491.7:c.1114A>G	ENSP00000377130.3:p.Ser372Gly
ENST00000393494.6:c.1669A>G	ENSP00000377132.2:p.Ser557Gly
ENST00000393498.6:c.1606A>G	ENSP00000377135.2:p.Ser536Gly
ENST00000403559.8:c.1720A>G	ENSP00000385069.4:p.Ser574Gly
ENST00000408937.7:c.1744A>G	ENSP00000386200.3:p.Ser582Gly
ENST00000412402.5:c.*1387A>G	ENSP00000405470.1:n.*1387A>G
ENST00000441290.6:c.*1669A>G	ENSP00000416825.1:n.*1669A>G
ENST00000634411.1:c.1618A>G	ENSP00000489135.1:p.Ser540Gly
ENST00000634623.1:c.1609A>G	ENSP00000488944.1:p.Ser537Gly
ENST00000634664.1:n.144A>G
ENST00000635109.1:c.*1466A>G	ENSP00000489457.1:n.*1466A>G
ENST00000635534.1:c.1660A>G	ENSP00000489229.1:p.Ser554Gly
ENST00000635638.1:c.1672A>G	ENSP00000489073.1:p.Ser558Gly
NM_001172766.2:c.1666A>G	NP_001166237.1:p.Ser556Gly
NM_014491.3:c.1669A>G	NP_055306.1:p.Ser557Gly
NM_148898.3:c.1744A>G	NP_683696.2:p.Ser582Gly
NM_148900.3:c.1720A>G	NP_683698.2:p.Ser574Gly
NR_033766.1:n.2054A>G
NR_033767.1:n.2101A>G
XM_011516706.1:c.1813A>G	XP_011515008.1:p.Ser605Gly
XM_017012801.2:c.1744A>G	XP_016868290.1:p.Ser582Gly
NM_014491.4:c.1669A>G MANE Select	NP_055306.1:p.Ser557Gly
NM_001172766.3:c.1666A>G	NP_001166237.1:p.Ser556Gly
NM_148898.4:c.1744A>G	NP_683696.2:p.Ser582Gly
NR_033766.2:n.2037A>G
NR_033767.2:n.2283A>G
NM_148900.4:c.1720A>G	NP_683698.2:p.Ser574Gly