Canonical Allele Identifier: CA457220275

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302212C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662157C>T , CM000669.2:g.114662157C>T	GRCh38
NC_000007.13:g.114302212C>T , CM000669.1:g.114302212C>T	GRCh37
NC_000007.12:g.114089448C>T	NCBI36
NG_007491.2:g.580848C>T
NG_007491.3:g.580848C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1791C>T	ENSP00000385069.4:p.Tyr597=
ENST00000703612.1:c.1731C>T	ENSP00000515396.1:p.Tyr577=
ENST00000703613.1:c.1791C>T	ENSP00000515397.1:p.Tyr597=
ENST00000703614.1:c.1740C>T	ENSP00000515398.1:p.Tyr580=
ENST00000703616.1:c.1866C>T	ENSP00000515400.1:p.Tyr622=
ENST00000703617.1:c.1185C>T	ENSP00000515401.1:p.Tyr395=
ENST00000703618.1:c.637C>T
ENST00000350908.9:c.1740C>T MANE Select	ENSP00000265436.7:p.Tyr580=
ENST00000393489.8:c.*1534C>T	ENSP00000377129.4:n.*1534C>T
ENST00000350908.8:c.1740C>T	ENSP00000265436.7:p.Tyr580=
ENST00000393489.7:c.1464C>T	ENSP00000377129.3:p.Tyr488=
ENST00000393491.7:c.1185C>T	ENSP00000377130.3:p.Tyr395=
ENST00000393494.6:c.1740C>T	ENSP00000377132.2:p.Tyr580=
ENST00000393498.6:c.1677C>T	ENSP00000377135.2:p.Tyr559=
ENST00000403559.8:c.1791C>T	ENSP00000385069.4:p.Tyr597=
ENST00000408937.7:c.1815C>T	ENSP00000386200.3:p.Tyr605=
ENST00000412402.5:c.*1458C>T	ENSP00000405470.1:n.*1458C>T
ENST00000441290.6:c.*1740C>T	ENSP00000416825.1:n.*1740C>T
ENST00000634411.1:c.1689C>T	ENSP00000489135.1:p.Tyr563=
ENST00000634623.1:c.1680C>T	ENSP00000488944.1:p.Tyr560=
ENST00000634664.1:n.215C>T
ENST00000635109.1:c.*1537C>T	ENSP00000489457.1:n.*1537C>T
ENST00000635534.1:c.1731C>T	ENSP00000489229.1:p.Tyr577=
ENST00000635638.1:c.1743C>T	ENSP00000489073.1:p.Tyr581=
NM_001172766.2:c.1737C>T	NP_001166237.1:p.Tyr579=
NM_014491.3:c.1740C>T	NP_055306.1:p.Tyr580=
NM_148898.3:c.1815C>T	NP_683696.2:p.Tyr605=
NM_148900.3:c.1791C>T	NP_683698.2:p.Tyr597=
NR_033766.1:n.2125C>T
NR_033767.1:n.2172C>T
XM_011516706.1:c.1884C>T	XP_011515008.1:p.Tyr628=
XM_017012801.2:c.1815C>T	XP_016868290.1:p.Tyr605=
NM_014491.4:c.1740C>T MANE Select	NP_055306.1:p.Tyr580=
NM_001172766.3:c.1737C>T	NP_001166237.1:p.Tyr579=
NM_148898.4:c.1815C>T	NP_683696.2:p.Tyr605=
NR_033766.2:n.2108C>T
NR_033767.2:n.2354C>T
NM_148900.4:c.1791C>T	NP_683698.2:p.Tyr597=