Canonical Allele Identifier: CA368965801

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302144C>A (hg19) ; chr7:g.114662089C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662089C>A , CM000669.2:g.114662089C>A	GRCh38
NC_000007.13:g.114302144C>A , CM000669.1:g.114302144C>A	GRCh37
NC_000007.12:g.114089380C>A	NCBI36
NG_007491.2:g.580780C>A
NG_007491.3:g.580780C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.1723C>A	ENSP00000385069.4:p.Leu575Met
ENST00000703612.1:c.1663C>A	ENSP00000515396.1:p.Leu555Met
ENST00000703613.1:c.1723C>A	ENSP00000515397.1:p.Leu575Met
ENST00000703614.1:c.1672C>A	ENSP00000515398.1:p.Leu558Met
ENST00000703616.1:c.1798C>A	ENSP00000515400.1:p.Leu600Met
ENST00000703617.1:c.1117C>A	ENSP00000515401.1:p.Leu373Met
ENST00000703618.1:c.569C>A
ENST00000350908.9:c.1672C>A MANE Select	ENSP00000265436.7:p.Leu558Met
ENST00000393489.8:c.*1466C>A	ENSP00000377129.4:n.*1466C>A
ENST00000350908.8:c.1672C>A	ENSP00000265436.7:p.Leu558Met
ENST00000393489.7:c.1396C>A	ENSP00000377129.3:p.Leu466Met
ENST00000393491.7:c.1117C>A	ENSP00000377130.3:p.Leu373Met
ENST00000393494.6:c.1672C>A	ENSP00000377132.2:p.Leu558Met
ENST00000393498.6:c.1609C>A	ENSP00000377135.2:p.Leu537Met
ENST00000403559.8:c.1723C>A	ENSP00000385069.4:p.Leu575Met
ENST00000408937.7:c.1747C>A	ENSP00000386200.3:p.Leu583Met
ENST00000412402.5:c.*1390C>A	ENSP00000405470.1:n.*1390C>A
ENST00000441290.6:c.*1672C>A	ENSP00000416825.1:n.*1672C>A
ENST00000634411.1:c.1621C>A	ENSP00000489135.1:p.Leu541Met
ENST00000634623.1:c.1612C>A	ENSP00000488944.1:p.Leu538Met
ENST00000634664.1:n.147C>A
ENST00000635109.1:c.*1469C>A	ENSP00000489457.1:n.*1469C>A
ENST00000635534.1:c.1663C>A	ENSP00000489229.1:p.Leu555Met
ENST00000635638.1:c.1675C>A	ENSP00000489073.1:p.Leu559Met
NM_001172766.2:c.1669C>A	NP_001166237.1:p.Leu557Met
NM_014491.3:c.1672C>A	NP_055306.1:p.Leu558Met
NM_148898.3:c.1747C>A	NP_683696.2:p.Leu583Met
NM_148900.3:c.1723C>A	NP_683698.2:p.Leu575Met
NR_033766.1:n.2057C>A
NR_033767.1:n.2104C>A
XM_011516706.1:c.1816C>A	XP_011515008.1:p.Leu606Met
XM_017012801.2:c.1747C>A	XP_016868290.1:p.Leu583Met
NM_014491.4:c.1672C>A MANE Select	NP_055306.1:p.Leu558Met
NM_001172766.3:c.1669C>A	NP_001166237.1:p.Leu557Met
NM_148898.4:c.1747C>A	NP_683696.2:p.Leu583Met
NR_033766.2:n.2040C>A
NR_033767.2:n.2286C>A
NM_148900.4:c.1723C>A	NP_683698.2:p.Leu575Met