Canonical Allele Identifier: CA1736046859
Gene: FOXP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.114659617T= , CM000669.2:g.114659617T= GRCh38
NC_000007.13:g.114299672T= , CM000669.1:g.114299672T= GRCh37
NC_000007.12:g.114086908T= NCBI36
NG_007491.2:g.578308T=
NG_007491.3:g.578308T=

Transcript Alleles

HGVS Amino-acid Change
NM_014491.4:c.1591T= MANE Select NP_055306.1:p.Tyr531=
ENST00000350908.9:c.1591T= MANE Select ENSP00000265436.7:p.Tyr531=
NM_001172766.2:c.1588T= NP_001166237.1:p.Tyr530=
NM_001172766.3:c.1588T= NP_001166237.1:p.Tyr530=
NM_014491.3:c.1591T= NP_055306.1:p.Tyr531=
NM_148898.3:c.1666T= NP_683696.2:p.Tyr556=
NM_148898.4:c.1666T= NP_683696.2:p.Tyr556=
NM_148900.3:c.1642T= NP_683698.2:p.Tyr548=
NM_148900.4:c.1642T= NP_683698.2:p.Tyr548=
NR_033766.1:n.1976T=
NR_033766.2:n.1959T=
NR_033767.1:n.2023T=
NR_033767.2:n.2205T=
ENST00000350908.8:c.1591T= ENSP00000265436.7:p.Tyr531=
ENST00000393489.7:c.1315T= ENSP00000377129.3:p.Tyr439=
ENST00000393489.8:c.*1385T= ENSP00000377129.4:n.*1385T=
ENST00000393491.7:c.1036T= ENSP00000377130.3:p.Tyr346=
ENST00000393494.6:c.1591T= ENSP00000377132.2:p.Tyr531=
ENST00000393498.6:c.1528T= ENSP00000377135.2:p.Tyr510=
ENST00000403559.8:c.1642T= ENSP00000385069.4:p.Tyr548=
ENST00000403559.9:c.1642T= ENSP00000385069.4:p.Tyr548=
ENST00000408937.7:c.1666T= ENSP00000386200.3:p.Tyr556=
ENST00000412402.5:c.*1309T= ENSP00000405470.1:n.*1309T=
ENST00000441290.6:c.*1591T= ENSP00000416825.1:n.*1591T=
ENST00000634411.1:c.1540T= ENSP00000489135.1:p.Tyr514=
ENST00000634623.1:c.1531T= ENSP00000488944.1:p.Tyr511=
ENST00000635109.1:c.*1388T= ENSP00000489457.1:n.*1388T=
ENST00000635534.1:c.1582T= ENSP00000489229.1:p.Tyr528=
ENST00000635638.1:c.1594T= ENSP00000489073.1:p.Tyr532=
ENST00000703612.1:c.1582T= ENSP00000515396.1:p.Tyr528=
ENST00000703613.1:c.1642T= ENSP00000515397.1:p.Tyr548=
ENST00000703614.1:c.1591T= ENSP00000515398.1:p.Tyr531=
ENST00000703616.1:c.1717T= ENSP00000515400.1:p.Tyr573=
ENST00000703617.1:c.1036T= ENSP00000515401.1:p.Tyr346=
ENST00000703618.1:c.545-2448T=
XM_011516706.1:c.1735T= XP_011515008.1:p.Tyr579=
XM_017012801.2:c.1666T= XP_016868290.1:p.Tyr556=