Canonical Allele Identifier: CA15500365
Gene: FOXP2 HGNC NCBI

Linked Data

dbSNP Id: rs2396753

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.114508276C>A , CM000669.2:g.114508276C>A GRCh38
NC_000007.13:g.114148331C>A , CM000669.1:g.114148331C>A GRCh37
NC_000007.12:g.113935567C>A NCBI36
NG_007491.2:g.426967C>A
NG_007491.3:g.426967C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000403559.9:c.169-26341C>A ENSP00000385069.4:n.169-26341C>A
ENST00000703612.1:c.169-26341C>A ENSP00000515396.1:n.169-26341C>A
ENST00000703613.1:c.169-26341C>A ENSP00000515397.1:n.169-26341C>A
ENST00000703614.1:c.169-26341C>A ENSP00000515398.1:n.169-26341C>A
ENST00000703615.1:c.169-26341C>A ENSP00000515399.1:n.169-26341C>A
ENST00000703616.1:c.169-26341C>A ENSP00000515400.1:n.169-26341C>A
ENST00000350908.9:c.169-26341C>A MANE Select ENSP00000265436.7:n.169-26341C>A
ENST00000393489.8:c.169-26341C>A ENSP00000377129.4:n.169-26341C>A
ENST00000350908.8:c.169-26341C>A ENSP00000265436.7:n.169-26341C>A
ENST00000360232.8:c.169-26341C>A ENSP00000353367.4:n.169-26341C>A
ENST00000378237.7:c.169-26341C>A ENSP00000367482.3:n.169-26341C>A
ENST00000390668.3:c.166-26341C>A ENSP00000375084.3:n.166-26341C>A
ENST00000393489.7:c.-166-26341C>A ENSP00000377129.3:n.-166-26341C>A
ENST00000393491.7:c.-108-26341C>A ENSP00000377130.3:n.-108-26341C>A
ENST00000393494.6:c.169-26341C>A ENSP00000377132.2:n.169-26341C>A
ENST00000393495.7:c.168+81597C>A ENSP00000377133.3:n.168+81597C>A
ENST00000393498.6:c.169-26341C>A ENSP00000377135.2:n.169-26341C>A
ENST00000403559.8:c.169-26341C>A ENSP00000385069.4:n.169-26341C>A
ENST00000408937.7:c.169-26341C>A ENSP00000386200.3:n.169-26341C>A
ENST00000412402.5:c.169-26341C>A ENSP00000405470.1:n.169-26341C>A
ENST00000440349.5:c.*228+9183C>A ENSP00000395552.1:n.*228+9183C>A
ENST00000441290.6:c.169-26341C>A ENSP00000416825.1:n.169-26341C>A
ENST00000452963.6:c.169-26341C>A ENSP00000409826.2:n.169-26341C>A
ENST00000459666.5:n.320-26341C>A
ENST00000634411.1:c.169-26341C>A ENSP00000489135.1:n.169-26341C>A
ENST00000634623.1:c.169-26341C>A ENSP00000488944.1:n.169-26341C>A
ENST00000635109.1:c.169-26341C>A ENSP00000489457.1:n.169-26341C>A
ENST00000635534.1:c.169-26341C>A ENSP00000489229.1:n.169-26341C>A
ENST00000635638.1:c.169-26341C>A ENSP00000489073.1:n.169-26341C>A
NM_001172766.2:c.169-26341C>A NP_001166237.1:n.169-26341C>A
NM_001172767.2:c.169-26341C>A NP_001166238.1:n.169-26341C>A
NM_014491.3:c.169-26341C>A NP_055306.1:n.169-26341C>A
NM_148898.3:c.169-26341C>A NP_683696.2:n.169-26341C>A
NM_148899.3:c.169-26341C>A NP_683697.2:n.169-26341C>A
NM_148900.3:c.169-26341C>A NP_683698.2:n.169-26341C>A
NR_033766.1:n.572-26341C>A
NR_033767.1:n.543-26341C>A
XM_011516706.1:c.169-26341C>A XP_011515008.1:n.169-26341C>A
XM_017012801.2:c.169-26341C>A XP_016868290.1:n.169-26341C>A
NM_014491.4:c.169-26341C>A MANE Select NP_055306.1:n.169-26341C>A
NM_001172766.3:c.169-26341C>A NP_001166237.1:n.169-26341C>A
NM_148898.4:c.169-26341C>A NP_683696.2:n.169-26341C>A
NR_033766.2:n.555-26341C>A
NR_033767.2:n.725-26341C>A
NM_148900.4:c.169-26341C>A NP_683698.2:n.169-26341C>A