Canonical Allele Identifier: CA1735785324
Gene: FOXP2 HGNC NCBI

Linked Data

dbSNP Id: rs1790933378

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.114100977T>G , CM000669.2:g.114100977T>G GRCh38
NC_000007.13:g.113741032T>G , CM000669.1:g.113741032T>G GRCh37
NC_000007.12:g.113528268T>G NCBI36
NG_007491.2:g.19668T>G
NG_007491.3:g.19668T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703612.1:c.-247+14366T>G ENSP00000515396.1:n.-247+14366T>G
ENST00000703613.1:c.-365+14366T>G ENSP00000515397.1:n.-365+14366T>G
ENST00000703614.1:c.-247+14366T>G ENSP00000515398.1:n.-247+14366T>G
ENST00000703615.1:c.-365+14366T>G ENSP00000515399.1:n.-365+14366T>G
ENST00000703616.1:c.-247+13139T>G ENSP00000515400.1:n.-247+13139T>G
ENST00000412402.5:c.-102+14366T>G ENSP00000405470.1:n.-102+14366T>G
ENST00000440349.5:c.-247+14366T>G ENSP00000395552.1:n.-247+14366T>G
ENST00000441290.6:c.-435+14366T>G ENSP00000416825.1:n.-435+14366T>G
ENST00000495516.1:n.105+12707T>G
ENST00000635638.1:c.-247+13139T>G ENSP00000489073.1:n.-247+13139T>G
NR_033766.1:n.302+14366T>G
XM_011516706.1:c.-360+14366T>G XP_011515008.1:n.-360+14366T>G
XM_017012801.2:c.-247+12549T>G XP_016868290.1:n.-247+12549T>G
NR_033766.2:n.285+14366T>G