Canonical Allele Identifier: CA368965638

Gene: FOXP2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1655C>A	ENSP00000385069.4:p.Thr552Lys
ENST00000703612.1:c.1595C>A	ENSP00000515396.1:p.Thr532Lys
ENST00000703613.1:c.1655C>A	ENSP00000515397.1:p.Thr552Lys
ENST00000703614.1:c.1604C>A	ENSP00000515398.1:p.Thr535Lys
ENST00000703616.1:c.1730C>A	ENSP00000515400.1:p.Thr577Lys
ENST00000703617.1:c.1049C>A	ENSP00000515401.1:p.Thr350Lys
ENST00000703618.1:c.545-2435C>A
ENST00000350908.9:c.1604C>A MANE Select	ENSP00000265436.7:p.Thr535Lys
ENST00000393489.8:c.*1398C>A	ENSP00000377129.4:n.*1398C>A
ENST00000350908.8:c.1604C>A	ENSP00000265436.7:p.Thr535Lys
ENST00000393489.7:c.1328C>A	ENSP00000377129.3:p.Thr443Lys
ENST00000393491.7:c.1049C>A	ENSP00000377130.3:p.Thr350Lys
ENST00000393494.6:c.1604C>A	ENSP00000377132.2:p.Thr535Lys
ENST00000393498.6:c.1541C>A	ENSP00000377135.2:p.Thr514Lys
ENST00000403559.8:c.1655C>A	ENSP00000385069.4:p.Thr552Lys
ENST00000408937.7:c.1679C>A	ENSP00000386200.3:p.Thr560Lys
ENST00000412402.5:c.*1322C>A	ENSP00000405470.1:n.*1322C>A
ENST00000441290.6:c.*1604C>A	ENSP00000416825.1:n.*1604C>A
ENST00000634411.1:c.1553C>A	ENSP00000489135.1:p.Thr518Lys
ENST00000634623.1:c.1544C>A	ENSP00000488944.1:p.Thr515Lys
ENST00000635109.1:c.*1401C>A	ENSP00000489457.1:n.*1401C>A
ENST00000635534.1:c.1595C>A	ENSP00000489229.1:p.Thr532Lys
ENST00000635638.1:c.1607C>A	ENSP00000489073.1:p.Thr536Lys
NM_001172766.2:c.1601C>A	NP_001166237.1:p.Thr534Lys
NM_014491.3:c.1604C>A	NP_055306.1:p.Thr535Lys
NM_148898.3:c.1679C>A	NP_683696.2:p.Thr560Lys
NM_148900.3:c.1655C>A	NP_683698.2:p.Thr552Lys
NR_033766.1:n.1989C>A
NR_033767.1:n.2036C>A
XM_011516706.1:c.1748C>A	XP_011515008.1:p.Thr583Lys
XM_017012801.2:c.1679C>A	XP_016868290.1:p.Thr560Lys
NM_014491.4:c.1604C>A MANE Select	NP_055306.1:p.Thr535Lys
NM_001172766.3:c.1601C>A	NP_001166237.1:p.Thr534Lys
NM_148898.4:c.1679C>A	NP_683696.2:p.Thr560Lys
NR_033766.2:n.1972C>A
NR_033767.2:n.2218C>A
NM_148900.4:c.1655C>A	NP_683698.2:p.Thr552Lys