Canonical Allele Identifier: CA368965912

Gene: FOXP2

Linked Data

• COSMIC: COSM1699222
• MyVariant Identifiers: chr7:g.114302193C>A (hg19) ; chr7:g.114662138C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662138C>A , CM000669.2:g.114662138C>A	GRCh38
NC_000007.13:g.114302193C>A , CM000669.1:g.114302193C>A	GRCh37
NC_000007.12:g.114089429C>A	NCBI36
NG_007491.2:g.580829C>A
NG_007491.3:g.580829C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1772C>A	ENSP00000385069.4:p.Thr591Asn
ENST00000703612.1:c.1712C>A	ENSP00000515396.1:p.Thr571Asn
ENST00000703613.1:c.1772C>A	ENSP00000515397.1:p.Thr591Asn
ENST00000703614.1:c.1721C>A	ENSP00000515398.1:p.Thr574Asn
ENST00000703616.1:c.1847C>A	ENSP00000515400.1:p.Thr616Asn
ENST00000703617.1:c.1166C>A	ENSP00000515401.1:p.Thr389Asn
ENST00000703618.1:c.618C>A
ENST00000350908.9:c.1721C>A MANE Select	ENSP00000265436.7:p.Thr574Asn
ENST00000393489.8:c.*1515C>A	ENSP00000377129.4:n.*1515C>A
ENST00000350908.8:c.1721C>A	ENSP00000265436.7:p.Thr574Asn
ENST00000393489.7:c.1445C>A	ENSP00000377129.3:p.Thr482Asn
ENST00000393491.7:c.1166C>A	ENSP00000377130.3:p.Thr389Asn
ENST00000393494.6:c.1721C>A	ENSP00000377132.2:p.Thr574Asn
ENST00000393498.6:c.1658C>A	ENSP00000377135.2:p.Thr553Asn
ENST00000403559.8:c.1772C>A	ENSP00000385069.4:p.Thr591Asn
ENST00000408937.7:c.1796C>A	ENSP00000386200.3:p.Thr599Asn
ENST00000412402.5:c.*1439C>A	ENSP00000405470.1:n.*1439C>A
ENST00000441290.6:c.*1721C>A	ENSP00000416825.1:n.*1721C>A
ENST00000634411.1:c.1670C>A	ENSP00000489135.1:p.Thr557Asn
ENST00000634623.1:c.1661C>A	ENSP00000488944.1:p.Thr554Asn
ENST00000634664.1:n.196C>A
ENST00000635109.1:c.*1518C>A	ENSP00000489457.1:n.*1518C>A
ENST00000635534.1:c.1712C>A	ENSP00000489229.1:p.Thr571Asn
ENST00000635638.1:c.1724C>A	ENSP00000489073.1:p.Thr575Asn
NM_001172766.2:c.1718C>A	NP_001166237.1:p.Thr573Asn
NM_014491.3:c.1721C>A	NP_055306.1:p.Thr574Asn
NM_148898.3:c.1796C>A	NP_683696.2:p.Thr599Asn
NM_148900.3:c.1772C>A	NP_683698.2:p.Thr591Asn
NR_033766.1:n.2106C>A
NR_033767.1:n.2153C>A
XM_011516706.1:c.1865C>A	XP_011515008.1:p.Thr622Asn
XM_017012801.2:c.1796C>A	XP_016868290.1:p.Thr599Asn
NM_014491.4:c.1721C>A MANE Select	NP_055306.1:p.Thr574Asn
NM_001172766.3:c.1718C>A	NP_001166237.1:p.Thr573Asn
NM_148898.4:c.1796C>A	NP_683696.2:p.Thr599Asn
NR_033766.2:n.2089C>A
NR_033767.2:n.2335C>A
NM_148900.4:c.1772C>A	NP_683698.2:p.Thr591Asn