Canonical Allele Identifier: CA15532051

Gene: FOXP2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114101050T>G , CM000669.2:g.114101050T>G	GRCh38
NC_000007.13:g.113741105T>G , CM000669.1:g.113741105T>G	GRCh37
NC_000007.12:g.113528341T>G	NCBI36
NG_007491.2:g.19741T>G
NG_007491.3:g.19741T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703612.1:c.-247+14439T>G	ENSP00000515396.1:n.-247+14439T>G
ENST00000703613.1:c.-365+14439T>G	ENSP00000515397.1:n.-365+14439T>G
ENST00000703614.1:c.-247+14439T>G	ENSP00000515398.1:n.-247+14439T>G
ENST00000703615.1:c.-365+14439T>G	ENSP00000515399.1:n.-365+14439T>G
ENST00000703616.1:c.-247+13212T>G	ENSP00000515400.1:n.-247+13212T>G
ENST00000412402.5:c.-102+14439T>G	ENSP00000405470.1:n.-102+14439T>G
ENST00000440349.5:c.-247+14439T>G	ENSP00000395552.1:n.-247+14439T>G
ENST00000441290.6:c.-435+14439T>G	ENSP00000416825.1:n.-435+14439T>G
ENST00000495516.1:n.105+12780T>G
ENST00000635638.1:c.-247+13212T>G	ENSP00000489073.1:n.-247+13212T>G
NR_033766.1:n.302+14439T>G
XM_011516706.1:c.-360+14439T>G	XP_011515008.1:n.-360+14439T>G
XM_017012801.2:c.-247+12622T>G	XP_016868290.1:n.-247+12622T>G
NR_033766.2:n.285+14439T>G