Canonical Allele Identifier: CA831841894

Gene: FOXP2

Linked Data

• dbSNP Id: rs1377643704
• gnomAD v3: 7-114662215-T-C
• gnomAD v4: 7-114662215-T-C
• MyVariant Identifiers: chr7:g.114302270T>C (hg19) ; chr7:g.114662215T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662215T>C , CM000669.2:g.114662215T>C	GRCh38
NC_000007.13:g.114302270T>C , CM000669.1:g.114302270T>C	GRCh37
NC_000007.12:g.114089506T>C	NCBI36
NG_007491.2:g.580906T>C
NG_007491.3:g.580906T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1820+29T>C	ENSP00000385069.4:n.1820+29T>C
ENST00000703612.1:c.1760+29T>C	ENSP00000515396.1:n.1760+29T>C
ENST00000703613.1:c.1820+29T>C	ENSP00000515397.1:n.1820+29T>C
ENST00000703614.1:c.1769+29T>C	ENSP00000515398.1:n.1769+29T>C
ENST00000703616.1:c.1895+29T>C	ENSP00000515400.1:n.1895+29T>C
ENST00000703617.1:c.1214+29T>C	ENSP00000515401.1:n.1214+29T>C
ENST00000703618.1:c.666+29T>C
ENST00000350908.9:c.1769+29T>C MANE Select	ENSP00000265436.7:n.1769+29T>C
ENST00000393489.8:c.*1563+29T>C	ENSP00000377129.4:n.*1563+29T>C
ENST00000350908.8:c.1769+29T>C	ENSP00000265436.7:n.1769+29T>C
ENST00000393489.7:c.1493+29T>C	ENSP00000377129.3:n.1493+29T>C
ENST00000393491.7:c.1214+29T>C	ENSP00000377130.3:n.1214+29T>C
ENST00000393494.6:c.1769+29T>C	ENSP00000377132.2:n.1769+29T>C
ENST00000393498.6:c.1706+29T>C	ENSP00000377135.2:n.1706+29T>C
ENST00000403559.8:c.1820+29T>C	ENSP00000385069.4:n.1820+29T>C
ENST00000408937.7:c.1844+29T>C	ENSP00000386200.3:n.1844+29T>C
ENST00000412402.5:c.*1487+29T>C	ENSP00000405470.1:n.*1487+29T>C
ENST00000441290.6:c.*1769+29T>C	ENSP00000416825.1:n.*1769+29T>C
ENST00000634411.1:c.1718+29T>C	ENSP00000489135.1:n.1718+29T>C
ENST00000634623.1:c.1709+29T>C	ENSP00000488944.1:n.1709+29T>C
ENST00000634664.1:n.244+29T>C
ENST00000635109.1:c.*1566+29T>C	ENSP00000489457.1:n.*1566+29T>C
ENST00000635534.1:c.1760+29T>C	ENSP00000489229.1:n.1760+29T>C
ENST00000635638.1:c.1772+29T>C	ENSP00000489073.1:n.1772+29T>C
NM_001172766.2:c.1766+29T>C	NP_001166237.1:n.1766+29T>C
NM_014491.3:c.1769+29T>C	NP_055306.1:n.1769+29T>C
NM_148898.3:c.1844+29T>C	NP_683696.2:n.1844+29T>C
NM_148900.3:c.1820+29T>C	NP_683698.2:n.1820+29T>C
NR_033766.1:n.2154+29T>C
NR_033767.1:n.2201+29T>C
XM_011516706.1:c.1913+29T>C	XP_011515008.1:n.1913+29T>C
XM_017012801.2:c.1844+29T>C	XP_016868290.1:n.1844+29T>C
NM_014491.4:c.1769+29T>C MANE Select	NP_055306.1:n.1769+29T>C
NM_001172766.3:c.1766+29T>C	NP_001166237.1:n.1766+29T>C
NM_148898.4:c.1844+29T>C	NP_683696.2:n.1844+29T>C
NR_033766.2:n.2137+29T>C
NR_033767.2:n.2383+29T>C
NM_148900.4:c.1820+29T>C	NP_683698.2:n.1820+29T>C