Canonical Allele Identifier: CA368965769

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302130G>T (hg19) ; chr7:g.114662075G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662075G>T , CM000669.2:g.114662075G>T	GRCh38
NC_000007.13:g.114302130G>T , CM000669.1:g.114302130G>T	GRCh37
NC_000007.12:g.114089366G>T	NCBI36
NG_007491.2:g.580766G>T
NG_007491.3:g.580766G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1709G>T	ENSP00000385069.4:p.Arg570Leu
ENST00000703612.1:c.1649G>T	ENSP00000515396.1:p.Arg550Leu
ENST00000703613.1:c.1709G>T	ENSP00000515397.1:p.Arg570Leu
ENST00000703614.1:c.1658G>T	ENSP00000515398.1:p.Arg553Leu
ENST00000703616.1:c.1784G>T	ENSP00000515400.1:p.Arg595Leu
ENST00000703617.1:c.1103G>T	ENSP00000515401.1:p.Arg368Leu
ENST00000703618.1:c.555G>T
ENST00000350908.9:c.1658G>T MANE Select	ENSP00000265436.7:p.Arg553Leu
ENST00000393489.8:c.*1452G>T	ENSP00000377129.4:n.*1452G>T
ENST00000350908.8:c.1658G>T	ENSP00000265436.7:p.Arg553Leu
ENST00000393489.7:c.1382G>T	ENSP00000377129.3:p.Arg461Leu
ENST00000393491.7:c.1103G>T	ENSP00000377130.3:p.Arg368Leu
ENST00000393494.6:c.1658G>T	ENSP00000377132.2:p.Arg553Leu
ENST00000393498.6:c.1595G>T	ENSP00000377135.2:p.Arg532Leu
ENST00000403559.8:c.1709G>T	ENSP00000385069.4:p.Arg570Leu
ENST00000408937.7:c.1733G>T	ENSP00000386200.3:p.Arg578Leu
ENST00000412402.5:c.*1376G>T	ENSP00000405470.1:n.*1376G>T
ENST00000441290.6:c.*1658G>T	ENSP00000416825.1:n.*1658G>T
ENST00000634411.1:c.1607G>T	ENSP00000489135.1:p.Arg536Leu
ENST00000634623.1:c.1598G>T	ENSP00000488944.1:p.Arg533Leu
ENST00000634664.1:n.133G>T
ENST00000635109.1:c.*1455G>T	ENSP00000489457.1:n.*1455G>T
ENST00000635534.1:c.1649G>T	ENSP00000489229.1:p.Arg550Leu
ENST00000635638.1:c.1661G>T	ENSP00000489073.1:p.Arg554Leu
NM_001172766.2:c.1655G>T	NP_001166237.1:p.Arg552Leu
NM_014491.3:c.1658G>T	NP_055306.1:p.Arg553Leu
NM_148898.3:c.1733G>T	NP_683696.2:p.Arg578Leu
NM_148900.3:c.1709G>T	NP_683698.2:p.Arg570Leu
NR_033766.1:n.2043G>T
NR_033767.1:n.2090G>T
XM_011516706.1:c.1802G>T	XP_011515008.1:p.Arg601Leu
XM_017012801.2:c.1733G>T	XP_016868290.1:p.Arg578Leu
NM_014491.4:c.1658G>T MANE Select	NP_055306.1:p.Arg553Leu
NM_001172766.3:c.1655G>T	NP_001166237.1:p.Arg552Leu
NM_148898.4:c.1733G>T	NP_683696.2:p.Arg578Leu
NR_033766.2:n.2026G>T
NR_033767.2:n.2272G>T
NM_148900.4:c.1709G>T	NP_683698.2:p.Arg570Leu