Canonical Allele Identifier: CA577211349

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114642810A>T , CM000669.2:g.114642810A>T	GRCh38
NC_000007.13:g.114282865A>T , CM000669.1:g.114282865A>T	GRCh37
NC_000007.12:g.114070101A>T	NCBI36
NG_007491.2:g.561501A>T
NG_007491.3:g.561501A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014491.4:c.989+187A>T MANE Select	NP_055306.1:n.989+187A>T
ENST00000350908.9:c.989+187A>T MANE Select	ENSP00000265436.7:n.989+187A>T
NM_001172766.2:c.986+187A>T	NP_001166237.1:n.986+187A>T
NM_001172766.3:c.986+187A>T	NP_001166237.1:n.986+187A>T
NM_001172767.2:c.1064+187A>T	NP_001166238.1:n.1064+187A>T
NM_014491.3:c.989+187A>T	NP_055306.1:n.989+187A>T
NM_148898.3:c.1064+187A>T	NP_683696.2:n.1064+187A>T
NM_148898.4:c.1064+187A>T	NP_683696.2:n.1064+187A>T
NM_148899.3:c.989+187A>T	NP_683697.2:n.989+187A>T
NM_148900.3:c.1040+187A>T	NP_683698.2:n.1040+187A>T
NM_148900.4:c.1040+187A>T	NP_683698.2:n.1040+187A>T
NR_033766.1:n.1576+187A>T
NR_033766.2:n.1559+187A>T
NR_033767.1:n.1421+187A>T
NR_033767.2:n.1603+187A>T
ENST00000350908.8:c.989+187A>T	ENSP00000265436.7:n.989+187A>T
ENST00000360232.8:c.989+187A>T	ENSP00000353367.4:n.989+187A>T
ENST00000378237.7:c.989+187A>T	ENSP00000367482.3:n.989+187A>T
ENST00000390668.3:c.1061+187A>T	ENSP00000375084.3:n.1061+187A>T
ENST00000393489.7:c.713+187A>T	ENSP00000377129.3:n.713+187A>T
ENST00000393489.8:c.*783+187A>T	ENSP00000377129.4:n.*783+187A>T
ENST00000393491.7:c.713+187A>T	ENSP00000377130.3:n.713+187A>T
ENST00000393494.6:c.989+187A>T	ENSP00000377132.2:n.989+187A>T
ENST00000393498.6:c.926+187A>T	ENSP00000377135.2:n.926+187A>T
ENST00000403559.8:c.1040+187A>T	ENSP00000385069.4:n.1040+187A>T
ENST00000403559.9:c.1040+187A>T	ENSP00000385069.4:n.1040+187A>T
ENST00000408937.7:c.1064+187A>T	ENSP00000386200.3:n.1064+187A>T
ENST00000412402.5:c.*909+187A>T	ENSP00000405470.1:n.*909+187A>T
ENST00000441290.6:c.*834+187A>T	ENSP00000416825.1:n.*834+187A>T
ENST00000634372.1:n.222-9393A>T
ENST00000634411.1:c.938+187A>T	ENSP00000489135.1:n.938+187A>T
ENST00000634623.1:c.929+187A>T	ENSP00000488944.1:n.929+187A>T
ENST00000635109.1:c.*786+187A>T	ENSP00000489457.1:n.*786+187A>T
ENST00000635534.1:c.980+187A>T	ENSP00000489229.1:n.980+187A>T
ENST00000635563.1:c.529+187A>T
ENST00000635638.1:c.992+187A>T	ENSP00000489073.1:n.992+187A>T
ENST00000703612.1:c.980+187A>T	ENSP00000515396.1:n.980+187A>T
ENST00000703613.1:c.1040+187A>T	ENSP00000515397.1:n.1040+187A>T
ENST00000703614.1:c.989+187A>T	ENSP00000515398.1:n.989+187A>T
ENST00000703616.1:c.1115+187A>T	ENSP00000515400.1:n.1115+187A>T
ENST00000703617.1:c.713+187A>T	ENSP00000515401.1:n.713+187A>T
ENST00000703618.1:c.267+187A>T
XM_011516706.1:c.1133+187A>T	XP_011515008.1:n.1133+187A>T
XM_017012801.2:c.1064+187A>T	XP_016868290.1:n.1064+187A>T