Canonical Allele Identifier: CA368966006

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114302233G>C (hg19) ; chr7:g.114662178G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114662178G>C , CM000669.2:g.114662178G>C	GRCh38
NC_000007.13:g.114302233G>C , CM000669.1:g.114302233G>C	GRCh37
NC_000007.12:g.114089469G>C	NCBI36
NG_007491.2:g.580869G>C
NG_007491.3:g.580869G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1812G>C	ENSP00000385069.4:p.Lys604Asn
ENST00000703612.1:c.1752G>C	ENSP00000515396.1:p.Lys584Asn
ENST00000703613.1:c.1812G>C	ENSP00000515397.1:p.Lys604Asn
ENST00000703614.1:c.1761G>C	ENSP00000515398.1:p.Lys587Asn
ENST00000703616.1:c.1887G>C	ENSP00000515400.1:p.Lys629Asn
ENST00000703617.1:c.1206G>C	ENSP00000515401.1:p.Lys402Asn
ENST00000703618.1:c.658G>C
ENST00000350908.9:c.1761G>C MANE Select	ENSP00000265436.7:p.Lys587Asn
ENST00000393489.8:c.*1555G>C	ENSP00000377129.4:n.*1555G>C
ENST00000350908.8:c.1761G>C	ENSP00000265436.7:p.Lys587Asn
ENST00000393489.7:c.1485G>C	ENSP00000377129.3:p.Lys495Asn
ENST00000393491.7:c.1206G>C	ENSP00000377130.3:p.Lys402Asn
ENST00000393494.6:c.1761G>C	ENSP00000377132.2:p.Lys587Asn
ENST00000393498.6:c.1698G>C	ENSP00000377135.2:p.Lys566Asn
ENST00000403559.8:c.1812G>C	ENSP00000385069.4:p.Lys604Asn
ENST00000408937.7:c.1836G>C	ENSP00000386200.3:p.Lys612Asn
ENST00000412402.5:c.*1479G>C	ENSP00000405470.1:n.*1479G>C
ENST00000441290.6:c.*1761G>C	ENSP00000416825.1:n.*1761G>C
ENST00000634411.1:c.1710G>C	ENSP00000489135.1:p.Lys570Asn
ENST00000634623.1:c.1701G>C	ENSP00000488944.1:p.Lys567Asn
ENST00000634664.1:n.236G>C
ENST00000635109.1:c.*1558G>C	ENSP00000489457.1:n.*1558G>C
ENST00000635534.1:c.1752G>C	ENSP00000489229.1:p.Lys584Asn
ENST00000635638.1:c.1764G>C	ENSP00000489073.1:p.Lys588Asn
NM_001172766.2:c.1758G>C	NP_001166237.1:p.Lys586Asn
NM_014491.3:c.1761G>C	NP_055306.1:p.Lys587Asn
NM_148898.3:c.1836G>C	NP_683696.2:p.Lys612Asn
NM_148900.3:c.1812G>C	NP_683698.2:p.Lys604Asn
NR_033766.1:n.2146G>C
NR_033767.1:n.2193G>C
XM_011516706.1:c.1905G>C	XP_011515008.1:p.Lys635Asn
XM_017012801.2:c.1836G>C	XP_016868290.1:p.Lys612Asn
NM_014491.4:c.1761G>C MANE Select	NP_055306.1:p.Lys587Asn
NM_001172766.3:c.1758G>C	NP_001166237.1:p.Lys586Asn
NM_148898.4:c.1836G>C	NP_683696.2:p.Lys612Asn
NR_033766.2:n.2129G>C
NR_033767.2:n.2375G>C
NM_148900.4:c.1812G>C	NP_683698.2:p.Lys604Asn