Canonical Allele Identifier: CA368965639

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299685C>G (hg19) ; chr7:g.114659630C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659630C>G , CM000669.2:g.114659630C>G	GRCh38
NC_000007.13:g.114299685C>G , CM000669.1:g.114299685C>G	GRCh37
NC_000007.12:g.114086921C>G	NCBI36
NG_007491.2:g.578321C>G
NG_007491.3:g.578321C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1655C>G	ENSP00000385069.4:p.Thr552Arg
ENST00000703612.1:c.1595C>G	ENSP00000515396.1:p.Thr532Arg
ENST00000703613.1:c.1655C>G	ENSP00000515397.1:p.Thr552Arg
ENST00000703614.1:c.1604C>G	ENSP00000515398.1:p.Thr535Arg
ENST00000703616.1:c.1730C>G	ENSP00000515400.1:p.Thr577Arg
ENST00000703617.1:c.1049C>G	ENSP00000515401.1:p.Thr350Arg
ENST00000703618.1:c.545-2435C>G
ENST00000350908.9:c.1604C>G MANE Select	ENSP00000265436.7:p.Thr535Arg
ENST00000393489.8:c.*1398C>G	ENSP00000377129.4:n.*1398C>G
ENST00000350908.8:c.1604C>G	ENSP00000265436.7:p.Thr535Arg
ENST00000393489.7:c.1328C>G	ENSP00000377129.3:p.Thr443Arg
ENST00000393491.7:c.1049C>G	ENSP00000377130.3:p.Thr350Arg
ENST00000393494.6:c.1604C>G	ENSP00000377132.2:p.Thr535Arg
ENST00000393498.6:c.1541C>G	ENSP00000377135.2:p.Thr514Arg
ENST00000403559.8:c.1655C>G	ENSP00000385069.4:p.Thr552Arg
ENST00000408937.7:c.1679C>G	ENSP00000386200.3:p.Thr560Arg
ENST00000412402.5:c.*1322C>G	ENSP00000405470.1:n.*1322C>G
ENST00000441290.6:c.*1604C>G	ENSP00000416825.1:n.*1604C>G
ENST00000634411.1:c.1553C>G	ENSP00000489135.1:p.Thr518Arg
ENST00000634623.1:c.1544C>G	ENSP00000488944.1:p.Thr515Arg
ENST00000635109.1:c.*1401C>G	ENSP00000489457.1:n.*1401C>G
ENST00000635534.1:c.1595C>G	ENSP00000489229.1:p.Thr532Arg
ENST00000635638.1:c.1607C>G	ENSP00000489073.1:p.Thr536Arg
NM_001172766.2:c.1601C>G	NP_001166237.1:p.Thr534Arg
NM_014491.3:c.1604C>G	NP_055306.1:p.Thr535Arg
NM_148898.3:c.1679C>G	NP_683696.2:p.Thr560Arg
NM_148900.3:c.1655C>G	NP_683698.2:p.Thr552Arg
NR_033766.1:n.1989C>G
NR_033767.1:n.2036C>G
XM_011516706.1:c.1748C>G	XP_011515008.1:p.Thr583Arg
XM_017012801.2:c.1679C>G	XP_016868290.1:p.Thr560Arg
NM_014491.4:c.1604C>G MANE Select	NP_055306.1:p.Thr535Arg
NM_001172766.3:c.1601C>G	NP_001166237.1:p.Thr534Arg
NM_148898.4:c.1679C>G	NP_683696.2:p.Thr560Arg
NR_033766.2:n.1972C>G
NR_033767.2:n.2218C>G
NM_148900.4:c.1655C>G	NP_683698.2:p.Thr552Arg