Canonical Allele Identifier: CA369105657

Gene: FOXP2

Linked Data

• dbSNP Id: rs1169006435
• MyVariant Identifiers: chr7:g.114066645T>A (hg19) ; chr7:g.114426590T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114426590T>A , CM000669.2:g.114426590T>A	GRCh38
NC_000007.13:g.114066645T>A , CM000669.1:g.114066645T>A	GRCh37
NC_000007.12:g.113853881T>A	NCBI36
NG_007491.2:g.345281T>A
NG_007491.3:g.345281T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403559.9:c.79T>A	ENSP00000385069.4:p.Leu27Ile
ENST00000703612.1:c.79T>A	ENSP00000515396.1:p.Leu27Ile
ENST00000703613.1:c.79T>A	ENSP00000515397.1:p.Leu27Ile
ENST00000703614.1:c.79T>A	ENSP00000515398.1:p.Leu27Ile
ENST00000703615.1:c.79T>A	ENSP00000515399.1:p.Leu27Ile
ENST00000703616.1:c.79T>A	ENSP00000515400.1:p.Leu27Ile
ENST00000350908.9:c.79T>A MANE Select	ENSP00000265436.7:p.Leu27Ile
ENST00000393489.8:c.79T>A	ENSP00000377129.4:p.Leu27Ile
ENST00000350908.8:c.79T>A	ENSP00000265436.7:p.Leu27Ile
ENST00000360232.8:c.79T>A	ENSP00000353367.4:p.Leu27Ile
ENST00000378237.7:c.79T>A	ENSP00000367482.3:p.Leu27Ile
ENST00000390668.3:c.76T>A	ENSP00000375084.3:p.Leu26Ile
ENST00000393489.7:c.-256T>A	ENSP00000377129.3:n.-256T>A
ENST00000393491.7:c.-198T>A	ENSP00000377130.3:n.-198T>A
ENST00000393494.6:c.79T>A	ENSP00000377132.2:p.Leu27Ile
ENST00000393495.7:c.79T>A	ENSP00000377133.3:p.Leu27Ile
ENST00000393498.6:c.79T>A	ENSP00000377135.2:p.Leu27Ile
ENST00000403559.8:c.79T>A	ENSP00000385069.4:p.Leu27Ile
ENST00000408937.7:c.79T>A	ENSP00000386200.3:p.Leu27Ile
ENST00000412402.5:c.79T>A	ENSP00000405470.1:p.Leu27Ile
ENST00000440349.5:c.79T>A	ENSP00000395552.1:p.Leu27Ile
ENST00000441290.6:c.79T>A	ENSP00000416825.1:p.Leu27Ile
ENST00000452963.6:c.79T>A	ENSP00000409826.2:p.Leu27Ile
ENST00000459666.5:n.230T>A
ENST00000462331.5:c.79T>A	ENSP00000418100.1:p.Leu27Ile
ENST00000634411.1:c.79T>A	ENSP00000489135.1:p.Leu27Ile
ENST00000634623.1:c.79T>A	ENSP00000488944.1:p.Leu27Ile
ENST00000635109.1:c.79T>A	ENSP00000489457.1:p.Leu27Ile
ENST00000635534.1:c.79T>A	ENSP00000489229.1:p.Leu27Ile
ENST00000635638.1:c.79T>A	ENSP00000489073.1:p.Leu27Ile
NM_001172766.2:c.79T>A	NP_001166237.1:p.Leu27Ile
NM_001172767.2:c.79T>A	NP_001166238.1:p.Leu27Ile
NM_014491.3:c.79T>A	NP_055306.1:p.Leu27Ile
NM_148898.3:c.79T>A	NP_683696.2:p.Leu27Ile
NM_148899.3:c.79T>A	NP_683697.2:p.Leu27Ile
NM_148900.3:c.79T>A	NP_683698.2:p.Leu27Ile
NR_033766.1:n.482T>A
NR_033767.1:n.453T>A
XM_011516706.1:c.79T>A	XP_011515008.1:p.Leu27Ile
XM_017012801.2:c.79T>A	XP_016868290.1:p.Leu27Ile
NM_014491.4:c.79T>A MANE Select	NP_055306.1:p.Leu27Ile
NM_001172766.3:c.79T>A	NP_001166237.1:p.Leu27Ile
NM_148898.4:c.79T>A	NP_683696.2:p.Leu27Ile
NR_033766.2:n.465T>A
NR_033767.2:n.635T>A
NM_148900.4:c.79T>A	NP_683698.2:p.Leu27Ile