Canonical Allele Identifier: CA1735785388
Gene: FOXP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.114101148C= , CM000669.2:g.114101148C= GRCh38
NC_000007.13:g.113741203C= , CM000669.1:g.113741203C= GRCh37
NC_000007.12:g.113528439C= NCBI36
NG_007491.2:g.19839C=
NG_007491.3:g.19839C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703612.1:c.-247+14537C= ENSP00000515396.1:n.-247+14537C=
ENST00000703613.1:c.-365+14537C= ENSP00000515397.1:n.-365+14537C=
ENST00000703614.1:c.-247+14537C= ENSP00000515398.1:n.-247+14537C=
ENST00000703615.1:c.-365+14537C= ENSP00000515399.1:n.-365+14537C=
ENST00000703616.1:c.-247+13310C= ENSP00000515400.1:n.-247+13310C=
ENST00000412402.5:c.-102+14537C= ENSP00000405470.1:n.-102+14537C=
ENST00000440349.5:c.-247+14537C= ENSP00000395552.1:n.-247+14537C=
ENST00000441290.6:c.-435+14537C= ENSP00000416825.1:n.-435+14537C=
ENST00000495516.1:n.105+12878C=
ENST00000635638.1:c.-247+13310C= ENSP00000489073.1:n.-247+13310C=
NR_033766.1:n.302+14537C=
XM_011516706.1:c.-360+14537C= XP_011515008.1:n.-360+14537C=
XM_017012801.2:c.-247+12720C= XP_016868290.1:n.-247+12720C=
NR_033766.2:n.285+14537C=