Canonical Allele Identifier: CA1735785393
Gene: FOXP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.114101167T= , CM000669.2:g.114101167T= GRCh38
NC_000007.13:g.113741222T= , CM000669.1:g.113741222T= GRCh37
NC_000007.12:g.113528458T= NCBI36
NG_007491.2:g.19858T=
NG_007491.3:g.19858T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703612.1:c.-247+14556T= ENSP00000515396.1:n.-247+14556T=
ENST00000703613.1:c.-365+14556T= ENSP00000515397.1:n.-365+14556T=
ENST00000703614.1:c.-247+14556T= ENSP00000515398.1:n.-247+14556T=
ENST00000703615.1:c.-365+14556T= ENSP00000515399.1:n.-365+14556T=
ENST00000703616.1:c.-247+13329T= ENSP00000515400.1:n.-247+13329T=
ENST00000412402.5:c.-102+14556T= ENSP00000405470.1:n.-102+14556T=
ENST00000440349.5:c.-247+14556T= ENSP00000395552.1:n.-247+14556T=
ENST00000441290.6:c.-435+14556T= ENSP00000416825.1:n.-435+14556T=
ENST00000495516.1:n.105+12897T=
ENST00000635638.1:c.-247+13329T= ENSP00000489073.1:n.-247+13329T=
NR_033766.1:n.302+14556T=
XM_011516706.1:c.-360+14556T= XP_011515008.1:n.-360+14556T=
XM_017012801.2:c.-247+12739T= XP_016868290.1:n.-247+12739T=
NR_033766.2:n.285+14556T=