Canonical Allele Identifier: CA368965506

Gene: FOXP2

Linked Data

• MyVariant Identifiers: chr7:g.114299631T>C (hg19) ; chr7:g.114659576T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114659576T>C , CM000669.2:g.114659576T>C	GRCh38
NC_000007.13:g.114299631T>C , CM000669.1:g.114299631T>C	GRCh37
NC_000007.12:g.114086867T>C	NCBI36
NG_007491.2:g.578267T>C
NG_007491.3:g.578267T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.1601T>C	ENSP00000385069.4:p.Ile534Thr
ENST00000703612.1:c.1541T>C	ENSP00000515396.1:p.Ile514Thr
ENST00000703613.1:c.1601T>C	ENSP00000515397.1:p.Ile534Thr
ENST00000703614.1:c.1550T>C	ENSP00000515398.1:p.Ile517Thr
ENST00000703616.1:c.1676T>C	ENSP00000515400.1:p.Ile559Thr
ENST00000703617.1:c.995T>C	ENSP00000515401.1:p.Ile332Thr
ENST00000703618.1:c.545-2489T>C
ENST00000350908.9:c.1550T>C MANE Select	ENSP00000265436.7:p.Ile517Thr
ENST00000393489.8:c.*1344T>C	ENSP00000377129.4:n.*1344T>C
ENST00000350908.8:c.1550T>C	ENSP00000265436.7:p.Ile517Thr
ENST00000393489.7:c.1274T>C	ENSP00000377129.3:p.Ile425Thr
ENST00000393491.7:c.995T>C	ENSP00000377130.3:p.Ile332Thr
ENST00000393494.6:c.1550T>C	ENSP00000377132.2:p.Ile517Thr
ENST00000393498.6:c.1487T>C	ENSP00000377135.2:p.Ile496Thr
ENST00000403559.8:c.1601T>C	ENSP00000385069.4:p.Ile534Thr
ENST00000408937.7:c.1625T>C	ENSP00000386200.3:p.Ile542Thr
ENST00000412402.5:c.*1268T>C	ENSP00000405470.1:n.*1268T>C
ENST00000441290.6:c.*1550T>C	ENSP00000416825.1:n.*1550T>C
ENST00000634411.1:c.1499T>C	ENSP00000489135.1:p.Ile500Thr
ENST00000634623.1:c.1490T>C	ENSP00000488944.1:p.Ile497Thr
ENST00000635109.1:c.*1347T>C	ENSP00000489457.1:n.*1347T>C
ENST00000635534.1:c.1541T>C	ENSP00000489229.1:p.Ile514Thr
ENST00000635638.1:c.1553T>C	ENSP00000489073.1:p.Ile518Thr
NM_001172766.2:c.1547T>C	NP_001166237.1:p.Ile516Thr
NM_014491.3:c.1550T>C	NP_055306.1:p.Ile517Thr
NM_148898.3:c.1625T>C	NP_683696.2:p.Ile542Thr
NM_148900.3:c.1601T>C	NP_683698.2:p.Ile534Thr
NR_033766.1:n.1935T>C
NR_033767.1:n.1982T>C
XM_011516706.1:c.1694T>C	XP_011515008.1:p.Ile565Thr
XM_017012801.2:c.1625T>C	XP_016868290.1:p.Ile542Thr
NM_014491.4:c.1550T>C MANE Select	NP_055306.1:p.Ile517Thr
NM_001172766.3:c.1547T>C	NP_001166237.1:p.Ile516Thr
NM_148898.4:c.1625T>C	NP_683696.2:p.Ile542Thr
NR_033766.2:n.1918T>C
NR_033767.2:n.2164T>C
NM_148900.4:c.1601T>C	NP_683698.2:p.Ile534Thr