Canonical Allele Identifier: CA368965735

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299729G>C (hg19) ; chr7:g.114659674G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659674G>C , CM000669.2:g.114659674G>C	GRCh38
NC_000007.13:g.114299729G>C , CM000669.1:g.114299729G>C	GRCh37
NC_000007.12:g.114086965G>C	NCBI36
NG_007491.2:g.578365G>C
NG_007491.3:g.578365G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1698+1G>C	ENSP00000385069.4:n.1698+1G>C
ENST00000703612.1:c.1638+1G>C	ENSP00000515396.1:n.1638+1G>C
ENST00000703613.1:c.1698+1G>C	ENSP00000515397.1:n.1698+1G>C
ENST00000703614.1:c.1647+1G>C	ENSP00000515398.1:n.1647+1G>C
ENST00000703616.1:c.1773+1G>C	ENSP00000515400.1:n.1773+1G>C
ENST00000703617.1:c.1092+1G>C	ENSP00000515401.1:n.1092+1G>C
ENST00000703618.1:c.545-2391G>C
ENST00000350908.9:c.1647+1G>C MANE Select	ENSP00000265436.7:n.1647+1G>C
ENST00000393489.8:c.*1441+1G>C	ENSP00000377129.4:n.*1441+1G>C
ENST00000350908.8:c.1647+1G>C	ENSP00000265436.7:n.1647+1G>C
ENST00000393489.7:c.1371+1G>C	ENSP00000377129.3:n.1371+1G>C
ENST00000393491.7:c.1092+1G>C	ENSP00000377130.3:n.1092+1G>C
ENST00000393494.6:c.1647+1G>C	ENSP00000377132.2:n.1647+1G>C
ENST00000393498.6:c.1584+1G>C	ENSP00000377135.2:n.1584+1G>C
ENST00000403559.8:c.1698+1G>C	ENSP00000385069.4:n.1698+1G>C
ENST00000408937.7:c.1722+1G>C	ENSP00000386200.3:n.1722+1G>C
ENST00000412402.5:c.*1365+1G>C	ENSP00000405470.1:n.*1365+1G>C
ENST00000441290.6:c.*1647+1G>C	ENSP00000416825.1:n.*1647+1G>C
ENST00000634411.1:c.1596+1G>C	ENSP00000489135.1:n.1596+1G>C
ENST00000634623.1:c.1587+1G>C	ENSP00000488944.1:n.1587+1G>C
ENST00000635109.1:c.*1444+1G>C	ENSP00000489457.1:n.*1444+1G>C
ENST00000635534.1:c.1638+1G>C	ENSP00000489229.1:n.1638+1G>C
ENST00000635638.1:c.1650+1G>C	ENSP00000489073.1:n.1650+1G>C
NM_001172766.2:c.1644+1G>C	NP_001166237.1:n.1644+1G>C
NM_014491.3:c.1647+1G>C	NP_055306.1:n.1647+1G>C
NM_148898.3:c.1722+1G>C	NP_683696.2:n.1722+1G>C
NM_148900.3:c.1698+1G>C	NP_683698.2:n.1698+1G>C
NR_033766.1:n.2032+1G>C
NR_033767.1:n.2079+1G>C
XM_011516706.1:c.1791+1G>C	XP_011515008.1:n.1791+1G>C
XM_017012801.2:c.1722+1G>C	XP_016868290.1:n.1722+1G>C
NM_014491.4:c.1647+1G>C MANE Select	NP_055306.1:n.1647+1G>C
NM_001172766.3:c.1644+1G>C	NP_001166237.1:n.1644+1G>C
NM_148898.4:c.1722+1G>C	NP_683696.2:n.1722+1G>C
NR_033766.2:n.2015+1G>C
NR_033767.2:n.2261+1G>C
NM_148900.4:c.1698+1G>C	NP_683698.2:n.1698+1G>C