Canonical Allele Identifier: CA4445636

Gene: FOXP2

Linked Data

• dbSNP Id: rs373286903
• ExAC: 7:114066566 C / T
• gnomAD v4: 7-114426511-C-T
• MyVariant Identifiers: chr7:g.114066566C>T (hg19) ; chr7:g.114426511C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114426511C>T , CM000669.2:g.114426511C>T	GRCh38
NC_000007.13:g.114066566C>T , CM000669.1:g.114066566C>T	GRCh37
NC_000007.12:g.113853802C>T	NCBI36
NG_007491.2:g.345202C>T
NG_007491.3:g.345202C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403559.9:c.-1C>T	ENSP00000385069.4:n.-1C>T
ENST00000703612.1:c.-1C>T	ENSP00000515396.1:n.-1C>T
ENST00000703613.1:c.-1C>T	ENSP00000515397.1:n.-1C>T
ENST00000703614.1:c.-1C>T	ENSP00000515398.1:n.-1C>T
ENST00000703615.1:c.-1C>T	ENSP00000515399.1:n.-1C>T
ENST00000703616.1:c.-1C>T	ENSP00000515400.1:n.-1C>T
ENST00000350908.9:c.-1C>T MANE Select	ENSP00000265436.7:n.-1C>T
ENST00000393489.8:c.-1C>T	ENSP00000377129.4:n.-1C>T
ENST00000350908.8:c.-1C>T	ENSP00000265436.7:n.-1C>T
ENST00000360232.8:c.-1C>T	ENSP00000353367.4:n.-1C>T
ENST00000378237.7:c.-1C>T	ENSP00000367482.3:n.-1C>T
ENST00000393489.7:c.-335C>T	ENSP00000377129.3:n.-335C>T
ENST00000393491.7:c.-277C>T	ENSP00000377130.3:n.-277C>T
ENST00000393494.6:c.-1C>T	ENSP00000377132.2:n.-1C>T
ENST00000393495.7:c.-1C>T	ENSP00000377133.3:n.-1C>T
ENST00000393498.6:c.-1C>T	ENSP00000377135.2:n.-1C>T
ENST00000403559.8:c.-1C>T	ENSP00000385069.4:n.-1C>T
ENST00000408937.7:c.-1C>T	ENSP00000386200.3:n.-1C>T
ENST00000412402.5:c.-1C>T	ENSP00000405470.1:n.-1C>T
ENST00000440349.5:c.-1C>T	ENSP00000395552.1:n.-1C>T
ENST00000441290.6:c.-1C>T	ENSP00000416825.1:n.-1C>T
ENST00000452963.6:c.-1C>T	ENSP00000409826.2:n.-1C>T
ENST00000459666.5:n.151C>T
ENST00000462331.5:c.-1C>T	ENSP00000418100.1:n.-1C>T
ENST00000634411.1:c.-1C>T	ENSP00000489135.1:n.-1C>T
ENST00000634623.1:c.-1C>T	ENSP00000488944.1:n.-1C>T
ENST00000635109.1:c.-1C>T	ENSP00000489457.1:n.-1C>T
ENST00000635534.1:c.-1C>T	ENSP00000489229.1:n.-1C>T
ENST00000635638.1:c.-1C>T	ENSP00000489073.1:n.-1C>T
NM_001172766.2:c.-1C>T	NP_001166237.1:n.-1C>T
NM_001172767.2:c.-1C>T	NP_001166238.1:n.-1C>T
NM_014491.3:c.-1C>T	NP_055306.1:n.-1C>T
NM_148898.3:c.-1C>T	NP_683696.2:n.-1C>T
NM_148899.3:c.-1C>T	NP_683697.2:n.-1C>T
NM_148900.3:c.-1C>T	NP_683698.2:n.-1C>T
NR_033766.1:n.403C>T
NR_033767.1:n.374C>T
XM_011516706.1:c.-1C>T	XP_011515008.1:n.-1C>T
XM_017012801.2:c.-1C>T	XP_016868290.1:n.-1C>T
NM_014491.4:c.-1C>T MANE Select	NP_055306.1:n.-1C>T
NM_001172766.3:c.-1C>T	NP_001166237.1:n.-1C>T
NM_148898.4:c.-1C>T	NP_683696.2:n.-1C>T
NR_033766.2:n.386C>T
NR_033767.2:n.556C>T
NM_148900.4:c.-1C>T	NP_683698.2:n.-1C>T