Canonical Allele Identifier: CA2777519926
Gene: FOXP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.114508197_114508198insTGTG , CM000669.2:g.114508197_114508198insTGTG GRCh38
NC_000007.13:g.114148252_114148253insTGTG , CM000669.1:g.114148252_114148253insTGTG GRCh37
NC_000007.12:g.113935488_113935489insTGTG NCBI36
NG_007491.2:g.426888_426889insTGTG
NG_007491.3:g.426888_426889insTGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000403559.9:c.169-26420_169-26419insTGTG ENSP00000385069.4:n.169-26420_169-26419insTGTG
ENST00000703612.1:c.169-26420_169-26419insTGTG ENSP00000515396.1:n.169-26420_169-26419insTGTG
ENST00000703613.1:c.169-26420_169-26419insTGTG ENSP00000515397.1:n.169-26420_169-26419insTGTG
ENST00000703614.1:c.169-26420_169-26419insTGTG ENSP00000515398.1:n.169-26420_169-26419insTGTG
ENST00000703615.1:c.169-26420_169-26419insTGTG ENSP00000515399.1:n.169-26420_169-26419insTGTG
ENST00000703616.1:c.169-26420_169-26419insTGTG ENSP00000515400.1:n.169-26420_169-26419insTGTG
ENST00000350908.9:c.169-26420_169-26419insTGTG MANE Select ENSP00000265436.7:n.169-26420_169-26419insTGTG
ENST00000393489.8:c.169-26420_169-26419insTGTG ENSP00000377129.4:n.169-26420_169-26419insTGTG
ENST00000350908.8:c.169-26420_169-26419insTGTG ENSP00000265436.7:n.169-26420_169-26419insTGTG
ENST00000360232.8:c.169-26420_169-26419insTGTG ENSP00000353367.4:n.169-26420_169-26419insTGTG
ENST00000378237.7:c.169-26420_169-26419insTGTG ENSP00000367482.3:n.169-26420_169-26419insTGTG
ENST00000390668.3:c.166-26420_166-26419insTGTG ENSP00000375084.3:n.166-26420_166-26419insTGTG
ENST00000393489.7:c.-166-26420_-166-26419insTGTG ENSP00000377129.3:n.-166-26420_-166-26419insTGTG
ENST00000393491.7:c.-108-26420_-108-26419insTGTG ENSP00000377130.3:n.-108-26420_-108-26419insTGTG
ENST00000393494.6:c.169-26420_169-26419insTGTG ENSP00000377132.2:n.169-26420_169-26419insTGTG
ENST00000393495.7:c.168+81518_168+81519insTGTG ENSP00000377133.3:n.168+81518_168+81519insTGTG
ENST00000393498.6:c.169-26420_169-26419insTGTG ENSP00000377135.2:n.169-26420_169-26419insTGTG
ENST00000403559.8:c.169-26420_169-26419insTGTG ENSP00000385069.4:n.169-26420_169-26419insTGTG
ENST00000408937.7:c.169-26420_169-26419insTGTG ENSP00000386200.3:n.169-26420_169-26419insTGTG
ENST00000412402.5:c.169-26420_169-26419insTGTG ENSP00000405470.1:n.169-26420_169-26419insTGTG
ENST00000440349.5:c.*228+9104_*228+9105insTGTG ENSP00000395552.1:n.*228+9104_*228+9105insTGTG
ENST00000441290.6:c.169-26420_169-26419insTGTG ENSP00000416825.1:n.169-26420_169-26419insTGTG
ENST00000452963.6:c.169-26420_169-26419insTGTG ENSP00000409826.2:n.169-26420_169-26419insTGTG
ENST00000459666.5:n.320-26420_320-26419insTGTG
ENST00000634411.1:c.169-26420_169-26419insTGTG ENSP00000489135.1:n.169-26420_169-26419insTGTG
ENST00000634623.1:c.169-26420_169-26419insTGTG ENSP00000488944.1:n.169-26420_169-26419insTGTG
ENST00000635109.1:c.169-26420_169-26419insTGTG ENSP00000489457.1:n.169-26420_169-26419insTGTG
ENST00000635534.1:c.169-26420_169-26419insTGTG ENSP00000489229.1:n.169-26420_169-26419insTGTG
ENST00000635638.1:c.169-26420_169-26419insTGTG ENSP00000489073.1:n.169-26420_169-26419insTGTG
NM_001172766.2:c.169-26420_169-26419insTGTG NP_001166237.1:n.169-26420_169-26419insTGTG
NM_001172767.2:c.169-26420_169-26419insTGTG NP_001166238.1:n.169-26420_169-26419insTGTG
NM_014491.3:c.169-26420_169-26419insTGTG NP_055306.1:n.169-26420_169-26419insTGTG
NM_148898.3:c.169-26420_169-26419insTGTG NP_683696.2:n.169-26420_169-26419insTGTG
NM_148899.3:c.169-26420_169-26419insTGTG NP_683697.2:n.169-26420_169-26419insTGTG
NM_148900.3:c.169-26420_169-26419insTGTG NP_683698.2:n.169-26420_169-26419insTGTG
NR_033766.1:n.572-26420_572-26419insTGTG
NR_033767.1:n.543-26420_543-26419insTGTG
XM_011516706.1:c.169-26420_169-26419insTGTG XP_011515008.1:n.169-26420_169-26419insTGTG
XM_017012801.2:c.169-26420_169-26419insTGTG XP_016868290.1:n.169-26420_169-26419insTGTG
NM_014491.4:c.169-26420_169-26419insTGTG MANE Select NP_055306.1:n.169-26420_169-26419insTGTG
NM_001172766.3:c.169-26420_169-26419insTGTG NP_001166237.1:n.169-26420_169-26419insTGTG
NM_148898.4:c.169-26420_169-26419insTGTG NP_683696.2:n.169-26420_169-26419insTGTG
NR_033766.2:n.555-26420_555-26419insTGTG
NR_033767.2:n.725-26420_725-26419insTGTG
NM_148900.4:c.169-26420_169-26419insTGTG NP_683698.2:n.169-26420_169-26419insTGTG