Canonical Allele Identifier: CA2549434747

Gene: FOXP2

Linked Data

• gnomAD v4: 7-114659685-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659685T>G , CM000669.2:g.114659685T>G	GRCh38
NC_000007.13:g.114299740T>G , CM000669.1:g.114299740T>G	GRCh37
NC_000007.12:g.114086976T>G	NCBI36
NG_007491.2:g.578376T>G
NG_007491.3:g.578376T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1698+12T>G	ENSP00000385069.4:n.1698+12T>G
ENST00000703612.1:c.1638+12T>G	ENSP00000515396.1:n.1638+12T>G
ENST00000703613.1:c.1698+12T>G	ENSP00000515397.1:n.1698+12T>G
ENST00000703614.1:c.1647+12T>G	ENSP00000515398.1:n.1647+12T>G
ENST00000703616.1:c.1773+12T>G	ENSP00000515400.1:n.1773+12T>G
ENST00000703617.1:c.1092+12T>G	ENSP00000515401.1:n.1092+12T>G
ENST00000703618.1:c.545-2380T>G
ENST00000350908.9:c.1647+12T>G MANE Select	ENSP00000265436.7:n.1647+12T>G
ENST00000393489.8:c.*1441+12T>G	ENSP00000377129.4:n.*1441+12T>G
ENST00000350908.8:c.1647+12T>G	ENSP00000265436.7:n.1647+12T>G
ENST00000393489.7:c.1371+12T>G	ENSP00000377129.3:n.1371+12T>G
ENST00000393491.7:c.1092+12T>G	ENSP00000377130.3:n.1092+12T>G
ENST00000393494.6:c.1647+12T>G	ENSP00000377132.2:n.1647+12T>G
ENST00000393498.6:c.1584+12T>G	ENSP00000377135.2:n.1584+12T>G
ENST00000403559.8:c.1698+12T>G	ENSP00000385069.4:n.1698+12T>G
ENST00000408937.7:c.1722+12T>G	ENSP00000386200.3:n.1722+12T>G
ENST00000412402.5:c.*1365+12T>G	ENSP00000405470.1:n.*1365+12T>G
ENST00000441290.6:c.*1647+12T>G	ENSP00000416825.1:n.*1647+12T>G
ENST00000634411.1:c.1596+12T>G	ENSP00000489135.1:n.1596+12T>G
ENST00000634623.1:c.1587+12T>G	ENSP00000488944.1:n.1587+12T>G
ENST00000635109.1:c.*1444+12T>G	ENSP00000489457.1:n.*1444+12T>G
ENST00000635534.1:c.1638+12T>G	ENSP00000489229.1:n.1638+12T>G
ENST00000635638.1:c.1650+12T>G	ENSP00000489073.1:n.1650+12T>G
NM_001172766.2:c.1644+12T>G	NP_001166237.1:n.1644+12T>G
NM_014491.3:c.1647+12T>G	NP_055306.1:n.1647+12T>G
NM_148898.3:c.1722+12T>G	NP_683696.2:n.1722+12T>G
NM_148900.3:c.1698+12T>G	NP_683698.2:n.1698+12T>G
NR_033766.1:n.2032+12T>G
NR_033767.1:n.2079+12T>G
XM_011516706.1:c.1791+12T>G	XP_011515008.1:n.1791+12T>G
XM_017012801.2:c.1722+12T>G	XP_016868290.1:n.1722+12T>G
NM_014491.4:c.1647+12T>G MANE Select	NP_055306.1:n.1647+12T>G
NM_001172766.3:c.1644+12T>G	NP_001166237.1:n.1644+12T>G
NM_148898.4:c.1722+12T>G	NP_683696.2:n.1722+12T>G
NR_033766.2:n.2015+12T>G
NR_033767.2:n.2261+12T>G
NM_148900.4:c.1698+12T>G	NP_683698.2:n.1698+12T>G