Canonical Allele Identifier: CA368965744

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302119G>C (hg19) ; chr7:g.114662064G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662064G>C , CM000669.2:g.114662064G>C	GRCh38
NC_000007.13:g.114302119G>C , CM000669.1:g.114302119G>C	GRCh37
NC_000007.12:g.114089355G>C	NCBI36
NG_007491.2:g.580755G>C
NG_007491.3:g.580755G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1699-1G>C	ENSP00000385069.4:n.1699-1G>C
ENST00000703612.1:c.1639-1G>C	ENSP00000515396.1:n.1639-1G>C
ENST00000703613.1:c.1699-1G>C	ENSP00000515397.1:n.1699-1G>C
ENST00000703614.1:c.1648-1G>C	ENSP00000515398.1:n.1648-1G>C
ENST00000703616.1:c.1774-1G>C	ENSP00000515400.1:n.1774-1G>C
ENST00000703617.1:c.1093-1G>C	ENSP00000515401.1:n.1093-1G>C
ENST00000703618.1:c.545-1G>C
ENST00000350908.9:c.1648-1G>C MANE Select	ENSP00000265436.7:n.1648-1G>C
ENST00000393489.8:c.*1442-1G>C	ENSP00000377129.4:n.*1442-1G>C
ENST00000350908.8:c.1648-1G>C	ENSP00000265436.7:n.1648-1G>C
ENST00000393489.7:c.1372-1G>C	ENSP00000377129.3:n.1372-1G>C
ENST00000393491.7:c.1093-1G>C	ENSP00000377130.3:n.1093-1G>C
ENST00000393494.6:c.1648-1G>C	ENSP00000377132.2:n.1648-1G>C
ENST00000393498.6:c.1585-1G>C	ENSP00000377135.2:n.1585-1G>C
ENST00000403559.8:c.1699-1G>C	ENSP00000385069.4:n.1699-1G>C
ENST00000408937.7:c.1723-1G>C	ENSP00000386200.3:n.1723-1G>C
ENST00000412402.5:c.*1366-1G>C	ENSP00000405470.1:n.*1366-1G>C
ENST00000441290.6:c.*1648-1G>C	ENSP00000416825.1:n.*1648-1G>C
ENST00000634411.1:c.1597-1G>C	ENSP00000489135.1:n.1597-1G>C
ENST00000634623.1:c.1588-1G>C	ENSP00000488944.1:n.1588-1G>C
ENST00000634664.1:n.123-1G>C
ENST00000635109.1:c.*1445-1G>C	ENSP00000489457.1:n.*1445-1G>C
ENST00000635534.1:c.1639-1G>C	ENSP00000489229.1:n.1639-1G>C
ENST00000635638.1:c.1651-1G>C	ENSP00000489073.1:n.1651-1G>C
NM_001172766.2:c.1645-1G>C	NP_001166237.1:n.1645-1G>C
NM_014491.3:c.1648-1G>C	NP_055306.1:n.1648-1G>C
NM_148898.3:c.1723-1G>C	NP_683696.2:n.1723-1G>C
NM_148900.3:c.1699-1G>C	NP_683698.2:n.1699-1G>C
NR_033766.1:n.2033-1G>C
NR_033767.1:n.2080-1G>C
XM_011516706.1:c.1792-1G>C	XP_011515008.1:n.1792-1G>C
XM_017012801.2:c.1723-1G>C	XP_016868290.1:n.1723-1G>C
NM_014491.4:c.1648-1G>C MANE Select	NP_055306.1:n.1648-1G>C
NM_001172766.3:c.1645-1G>C	NP_001166237.1:n.1645-1G>C
NM_148898.4:c.1723-1G>C	NP_683696.2:n.1723-1G>C
NR_033766.2:n.2016-1G>C
NR_033767.2:n.2262-1G>C
NM_148900.4:c.1699-1G>C	NP_683698.2:n.1699-1G>C