Canonical Allele Identifier: CA1736046845
Gene: FOXP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.114659552T= , CM000669.2:g.114659552T= GRCh38
NC_000007.13:g.114299607T= , CM000669.1:g.114299607T= GRCh37
NC_000007.12:g.114086843T= NCBI36
NG_007491.2:g.578243T=
NG_007491.3:g.578243T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403559.9:c.1597-20T= ENSP00000385069.4:n.1597-20T=
ENST00000703612.1:c.1537-20T= ENSP00000515396.1:n.1537-20T=
ENST00000703613.1:c.1597-20T= ENSP00000515397.1:n.1597-20T=
ENST00000703614.1:c.1546-20T= ENSP00000515398.1:n.1546-20T=
ENST00000703616.1:c.1672-20T= ENSP00000515400.1:n.1672-20T=
ENST00000703617.1:c.991-20T= ENSP00000515401.1:n.991-20T=
ENST00000703618.1:c.545-2513T=
ENST00000350908.9:c.1546-20T= MANE Select ENSP00000265436.7:n.1546-20T=
ENST00000393489.8:c.*1340-20T= ENSP00000377129.4:n.*1340-20T=
ENST00000350908.8:c.1546-20T= ENSP00000265436.7:n.1546-20T=
ENST00000393489.7:c.1270-20T= ENSP00000377129.3:n.1270-20T=
ENST00000393491.7:c.991-20T= ENSP00000377130.3:n.991-20T=
ENST00000393494.6:c.1546-20T= ENSP00000377132.2:n.1546-20T=
ENST00000393498.6:c.1483-20T= ENSP00000377135.2:n.1483-20T=
ENST00000403559.8:c.1597-20T= ENSP00000385069.4:n.1597-20T=
ENST00000408937.7:c.1621-20T= ENSP00000386200.3:n.1621-20T=
ENST00000412402.5:c.*1264-20T= ENSP00000405470.1:n.*1264-20T=
ENST00000441290.6:c.*1546-20T= ENSP00000416825.1:n.*1546-20T=
ENST00000634411.1:c.1495-20T= ENSP00000489135.1:n.1495-20T=
ENST00000634623.1:c.1486-20T= ENSP00000488944.1:n.1486-20T=
ENST00000635109.1:c.*1343-20T= ENSP00000489457.1:n.*1343-20T=
ENST00000635534.1:c.1537-20T= ENSP00000489229.1:n.1537-20T=
ENST00000635638.1:c.1549-20T= ENSP00000489073.1:n.1549-20T=
NM_001172766.2:c.1543-20T= NP_001166237.1:n.1543-20T=
NM_014491.3:c.1546-20T= NP_055306.1:n.1546-20T=
NM_148898.3:c.1621-20T= NP_683696.2:n.1621-20T=
NM_148900.3:c.1597-20T= NP_683698.2:n.1597-20T=
NR_033766.1:n.1931-20T=
NR_033767.1:n.1978-20T=
XM_011516706.1:c.1690-20T= XP_011515008.1:n.1690-20T=
XM_017012801.2:c.1621-20T= XP_016868290.1:n.1621-20T=
NM_014491.4:c.1546-20T= MANE Select NP_055306.1:n.1546-20T=
NM_001172766.3:c.1543-20T= NP_001166237.1:n.1543-20T=
NM_148898.4:c.1621-20T= NP_683696.2:n.1621-20T=
NR_033766.2:n.1914-20T=
NR_033767.2:n.2160-20T=
NM_148900.4:c.1597-20T= NP_683698.2:n.1597-20T=