Canonical Allele Identifier: CA368965768

Gene: FOXP2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1709G>C	ENSP00000385069.4:p.Arg570Pro
ENST00000703612.1:c.1649G>C	ENSP00000515396.1:p.Arg550Pro
ENST00000703613.1:c.1709G>C	ENSP00000515397.1:p.Arg570Pro
ENST00000703614.1:c.1658G>C	ENSP00000515398.1:p.Arg553Pro
ENST00000703616.1:c.1784G>C	ENSP00000515400.1:p.Arg595Pro
ENST00000703617.1:c.1103G>C	ENSP00000515401.1:p.Arg368Pro
ENST00000703618.1:c.555G>C
ENST00000350908.9:c.1658G>C MANE Select	ENSP00000265436.7:p.Arg553Pro
ENST00000393489.8:c.*1452G>C	ENSP00000377129.4:n.*1452G>C
ENST00000350908.8:c.1658G>C	ENSP00000265436.7:p.Arg553Pro
ENST00000393489.7:c.1382G>C	ENSP00000377129.3:p.Arg461Pro
ENST00000393491.7:c.1103G>C	ENSP00000377130.3:p.Arg368Pro
ENST00000393494.6:c.1658G>C	ENSP00000377132.2:p.Arg553Pro
ENST00000393498.6:c.1595G>C	ENSP00000377135.2:p.Arg532Pro
ENST00000403559.8:c.1709G>C	ENSP00000385069.4:p.Arg570Pro
ENST00000408937.7:c.1733G>C	ENSP00000386200.3:p.Arg578Pro
ENST00000412402.5:c.*1376G>C	ENSP00000405470.1:n.*1376G>C
ENST00000441290.6:c.*1658G>C	ENSP00000416825.1:n.*1658G>C
ENST00000634411.1:c.1607G>C	ENSP00000489135.1:p.Arg536Pro
ENST00000634623.1:c.1598G>C	ENSP00000488944.1:p.Arg533Pro
ENST00000634664.1:n.133G>C
ENST00000635109.1:c.*1455G>C	ENSP00000489457.1:n.*1455G>C
ENST00000635534.1:c.1649G>C	ENSP00000489229.1:p.Arg550Pro
ENST00000635638.1:c.1661G>C	ENSP00000489073.1:p.Arg554Pro
NM_001172766.2:c.1655G>C	NP_001166237.1:p.Arg552Pro
NM_014491.3:c.1658G>C	NP_055306.1:p.Arg553Pro
NM_148898.3:c.1733G>C	NP_683696.2:p.Arg578Pro
NM_148900.3:c.1709G>C	NP_683698.2:p.Arg570Pro
NR_033766.1:n.2043G>C
NR_033767.1:n.2090G>C
XM_011516706.1:c.1802G>C	XP_011515008.1:p.Arg601Pro
XM_017012801.2:c.1733G>C	XP_016868290.1:p.Arg578Pro
NM_014491.4:c.1658G>C MANE Select	NP_055306.1:p.Arg553Pro
NM_001172766.3:c.1655G>C	NP_001166237.1:p.Arg552Pro
NM_148898.4:c.1733G>C	NP_683696.2:p.Arg578Pro
NR_033766.2:n.2026G>C
NR_033767.2:n.2272G>C
NM_148900.4:c.1709G>C	NP_683698.2:p.Arg570Pro