Canonical Allele Identifier: CA368965698

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299713T>G (hg19) ; chr7:g.114659658T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659658T>G , CM000669.2:g.114659658T>G	GRCh38
NC_000007.13:g.114299713T>G , CM000669.1:g.114299713T>G	GRCh37
NC_000007.12:g.114086949T>G	NCBI36
NG_007491.2:g.578349T>G
NG_007491.3:g.578349T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1683T>G	ENSP00000385069.4:p.Asn561Lys
ENST00000703612.1:c.1623T>G	ENSP00000515396.1:p.Asn541Lys
ENST00000703613.1:c.1683T>G	ENSP00000515397.1:p.Asn561Lys
ENST00000703614.1:c.1632T>G	ENSP00000515398.1:p.Asn544Lys
ENST00000703616.1:c.1758T>G	ENSP00000515400.1:p.Asn586Lys
ENST00000703617.1:c.1077T>G	ENSP00000515401.1:p.Asn359Lys
ENST00000703618.1:c.545-2407T>G
ENST00000350908.9:c.1632T>G MANE Select	ENSP00000265436.7:p.Asn544Lys
ENST00000393489.8:c.*1426T>G	ENSP00000377129.4:n.*1426T>G
ENST00000350908.8:c.1632T>G	ENSP00000265436.7:p.Asn544Lys
ENST00000393489.7:c.1356T>G	ENSP00000377129.3:p.Asn452Lys
ENST00000393491.7:c.1077T>G	ENSP00000377130.3:p.Asn359Lys
ENST00000393494.6:c.1632T>G	ENSP00000377132.2:p.Asn544Lys
ENST00000393498.6:c.1569T>G	ENSP00000377135.2:p.Asn523Lys
ENST00000403559.8:c.1683T>G	ENSP00000385069.4:p.Asn561Lys
ENST00000408937.7:c.1707T>G	ENSP00000386200.3:p.Asn569Lys
ENST00000412402.5:c.*1350T>G	ENSP00000405470.1:n.*1350T>G
ENST00000441290.6:c.*1632T>G	ENSP00000416825.1:n.*1632T>G
ENST00000634411.1:c.1581T>G	ENSP00000489135.1:p.Asn527Lys
ENST00000634623.1:c.1572T>G	ENSP00000488944.1:p.Asn524Lys
ENST00000635109.1:c.*1429T>G	ENSP00000489457.1:n.*1429T>G
ENST00000635534.1:c.1623T>G	ENSP00000489229.1:p.Asn541Lys
ENST00000635638.1:c.1635T>G	ENSP00000489073.1:p.Asn545Lys
NM_001172766.2:c.1629T>G	NP_001166237.1:p.Asn543Lys
NM_014491.3:c.1632T>G	NP_055306.1:p.Asn544Lys
NM_148898.3:c.1707T>G	NP_683696.2:p.Asn569Lys
NM_148900.3:c.1683T>G	NP_683698.2:p.Asn561Lys
NR_033766.1:n.2017T>G
NR_033767.1:n.2064T>G
XM_011516706.1:c.1776T>G	XP_011515008.1:p.Asn592Lys
XM_017012801.2:c.1707T>G	XP_016868290.1:p.Asn569Lys
NM_014491.4:c.1632T>G MANE Select	NP_055306.1:p.Asn544Lys
NM_001172766.3:c.1629T>G	NP_001166237.1:p.Asn543Lys
NM_148898.4:c.1707T>G	NP_683696.2:p.Asn569Lys
NR_033766.2:n.2000T>G
NR_033767.2:n.2246T>G
NM_148900.4:c.1683T>G	NP_683698.2:p.Asn561Lys