Canonical Allele Identifier: CA368964150

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114292259C>G (hg19) ; chr7:g.114652204C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114652204C>G , CM000669.2:g.114652204C>G	GRCh38
NC_000007.13:g.114292259C>G , CM000669.1:g.114292259C>G	GRCh37
NC_000007.12:g.114079495C>G	NCBI36
NG_007491.2:g.570895C>G
NG_007491.3:g.570895C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1147C>G	ENSP00000385069.4:p.His383Asp
ENST00000703612.1:c.1087C>G	ENSP00000515396.1:p.His363Asp
ENST00000703613.1:c.1147C>G	ENSP00000515397.1:p.His383Asp
ENST00000703614.1:c.1096C>G	ENSP00000515398.1:p.His366Asp
ENST00000703616.1:c.1222C>G	ENSP00000515400.1:p.His408Asp
ENST00000703617.1:c.820C>G	ENSP00000515401.1:p.His274Asp
ENST00000703618.1:c.374C>G
ENST00000350908.9:c.1096C>G MANE Select	ENSP00000265436.7:p.His366Asp
ENST00000393489.8:c.*890C>G	ENSP00000377129.4:n.*890C>G
ENST00000350908.8:c.1096C>G	ENSP00000265436.7:p.His366Asp
ENST00000360232.8:c.1096C>G	ENSP00000353367.4:p.His366Asp
ENST00000390668.3:c.1168C>G	ENSP00000375084.3:p.His390Asp
ENST00000393489.7:c.820C>G	ENSP00000377129.3:p.His274Asp
ENST00000393491.7:c.820C>G	ENSP00000377130.3:p.His274Asp
ENST00000393494.6:c.1096C>G	ENSP00000377132.2:p.His366Asp
ENST00000393498.6:c.1033C>G	ENSP00000377135.2:p.His345Asp
ENST00000403559.8:c.1147C>G	ENSP00000385069.4:p.His383Asp
ENST00000408937.7:c.1171C>G	ENSP00000386200.3:p.His391Asp
ENST00000412402.5:c.*1016C>G	ENSP00000405470.1:n.*1016C>G
ENST00000441290.6:c.*941C>G	ENSP00000416825.1:n.*941C>G
ENST00000634372.1:n.223C>G
ENST00000634411.1:c.1045C>G	ENSP00000489135.1:p.His349Asp
ENST00000634623.1:c.1036C>G	ENSP00000488944.1:p.His346Asp
ENST00000635109.1:c.*893C>G	ENSP00000489457.1:n.*893C>G
ENST00000635534.1:c.1087C>G	ENSP00000489229.1:p.His363Asp
ENST00000635563.1:c.636C>G
ENST00000635638.1:c.1099C>G	ENSP00000489073.1:p.His367Asp
NM_001172766.2:c.1093C>G	NP_001166237.1:p.His365Asp
NM_001172767.2:c.1171C>G	NP_001166238.1:p.His391Asp
NM_014491.3:c.1096C>G	NP_055306.1:p.His366Asp
NM_148898.3:c.1171C>G	NP_683696.2:p.His391Asp
NM_148899.3:c.1096C>G	NP_683697.2:p.His366Asp
NM_148900.3:c.1147C>G	NP_683698.2:p.His383Asp
NR_033766.1:n.1683C>G
NR_033767.1:n.1528C>G
XM_011516706.1:c.1240C>G	XP_011515008.1:p.His414Asp
XM_017012801.2:c.1171C>G	XP_016868290.1:p.His391Asp
NM_014491.4:c.1096C>G MANE Select	NP_055306.1:p.His366Asp
NM_001172766.3:c.1093C>G	NP_001166237.1:p.His365Asp
NM_148898.4:c.1171C>G	NP_683696.2:p.His391Asp
NR_033766.2:n.1666C>G
NR_033767.2:n.1710C>G
NM_148900.4:c.1147C>G	NP_683698.2:p.His383Asp