Canonical Allele Identifier: CA831865501

Gene: FOXP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114630022T>C , CM000669.2:g.114630022T>C	GRCh38
NC_000007.13:g.114270077T>C , CM000669.1:g.114270077T>C	GRCh37
NC_000007.12:g.114057313T>C	NCBI36
NG_007491.2:g.548713T>C
NG_007491.3:g.548713T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.648+17T>C	ENSP00000385069.4:n.648+17T>C
ENST00000703612.1:c.588+17T>C	ENSP00000515396.1:n.588+17T>C
ENST00000703613.1:c.648+17T>C	ENSP00000515397.1:n.648+17T>C
ENST00000703614.1:c.597+17T>C	ENSP00000515398.1:n.597+17T>C
ENST00000703616.1:c.723+17T>C	ENSP00000515400.1:n.723+17T>C
ENST00000703617.1:c.321+17T>C	ENSP00000515401.1:n.321+17T>C
ENST00000350908.9:c.597+17T>C MANE Select	ENSP00000265436.7:n.597+17T>C
ENST00000393489.8:c.*391+17T>C	ENSP00000377129.4:n.*391+17T>C
ENST00000638397.1:c.130+34T>C	ENSP00000492698.1:n.130+34T>C
ENST00000350908.8:c.597+17T>C	ENSP00000265436.7:n.597+17T>C
ENST00000360232.8:c.597+17T>C	ENSP00000353367.4:n.597+17T>C
ENST00000378237.7:c.597+17T>C	ENSP00000367482.3:n.597+17T>C
ENST00000390668.3:c.669+17T>C	ENSP00000375084.3:n.669+17T>C
ENST00000393489.7:c.321+17T>C	ENSP00000377129.3:n.321+17T>C
ENST00000393491.7:c.321+17T>C	ENSP00000377130.3:n.321+17T>C
ENST00000393494.6:c.597+17T>C	ENSP00000377132.2:n.597+17T>C
ENST00000393495.7:c.169-1515T>C	ENSP00000377133.3:n.169-1515T>C
ENST00000393498.6:c.537+17T>C	ENSP00000377135.2:n.537+17T>C
ENST00000403559.8:c.648+17T>C	ENSP00000385069.4:n.648+17T>C
ENST00000408937.7:c.672+17T>C	ENSP00000386200.3:n.672+17T>C
ENST00000412402.5:c.*517+17T>C	ENSP00000405470.1:n.*517+17T>C
ENST00000440349.5:c.*784+17T>C	ENSP00000395552.1:n.*784+17T>C
ENST00000441290.6:c.*442+17T>C	ENSP00000416825.1:n.*442+17T>C
ENST00000634372.1:n.61+17T>C
ENST00000634411.1:c.546+17T>C	ENSP00000489135.1:n.546+17T>C
ENST00000634623.1:c.534+17T>C	ENSP00000488944.1:n.534+17T>C
ENST00000635109.1:c.*391+17T>C	ENSP00000489457.1:n.*391+17T>C
ENST00000635534.1:c.588+17T>C	ENSP00000489229.1:n.588+17T>C
ENST00000635563.1:c.152+17T>C
ENST00000635638.1:c.597+17T>C	ENSP00000489073.1:n.597+17T>C
NM_001172766.2:c.597+17T>C	NP_001166237.1:n.597+17T>C
NM_001172767.2:c.672+17T>C	NP_001166238.1:n.672+17T>C
NM_014491.3:c.597+17T>C	NP_055306.1:n.597+17T>C
NM_148898.3:c.672+17T>C	NP_683696.2:n.672+17T>C
NM_148899.3:c.597+17T>C	NP_683697.2:n.597+17T>C
NM_148900.3:c.648+17T>C	NP_683698.2:n.648+17T>C
NR_033766.1:n.1184+17T>C
NR_033767.1:n.1029+17T>C
XM_011516706.1:c.741+17T>C	XP_011515008.1:n.741+17T>C
XM_017012801.2:c.672+17T>C	XP_016868290.1:n.672+17T>C
NM_014491.4:c.597+17T>C MANE Select	NP_055306.1:n.597+17T>C
NM_001172766.3:c.597+17T>C	NP_001166237.1:n.597+17T>C
NM_148898.4:c.672+17T>C	NP_683696.2:n.672+17T>C
NR_033766.2:n.1167+17T>C
NR_033767.2:n.1211+17T>C
NM_148900.4:c.648+17T>C	NP_683698.2:n.648+17T>C