Canonical Allele Identifier: CA4446370

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114690162A>G , CM000669.2:g.114690162A>G	GRCh38
NC_000007.13:g.114330217A>G , CM000669.1:g.114330217A>G	GRCh37
NC_000007.12:g.114117453A>G	NCBI36
NG_007491.2:g.608853A>G
NG_007491.3:g.608853A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014491.4:c.*236A>G MANE Select	NP_055306.1:n.*236A>G
ENST00000350908.9:c.*236A>G MANE Select	ENSP00000265436.7:n.*236A>G
NM_001172766.2:c.*236A>G	NP_001166237.1:n.*236A>G
NM_001172766.3:c.*236A>G	NP_001166237.1:n.*236A>G
NM_014491.3:c.*236A>G	NP_055306.1:n.*236A>G
NM_148898.3:c.*236A>G	NP_683696.2:n.*236A>G
NM_148898.4:c.*236A>G	NP_683696.2:n.*236A>G
NM_148900.3:c.*236A>G	NP_683698.2:n.*236A>G
NM_148900.4:c.*236A>G	NP_683698.2:n.*236A>G
NR_033766.1:n.2769A>G
NR_033766.2:n.2752A>G
NR_033767.1:n.2816A>G
NR_033767.2:n.2998A>G
ENST00000393491.7:c.*236A>G	ENSP00000377130.3:n.*236A>G
ENST00000393494.6:c.*236A>G	ENSP00000377132.2:n.*236A>G
ENST00000403559.8:c.*236A>G	ENSP00000385069.4:n.*236A>G
ENST00000403559.9:c.*236A>G	ENSP00000385069.4:n.*236A>G
ENST00000408937.7:c.*236A>G	ENSP00000386200.3:n.*236A>G
ENST00000412402.5:c.*2102A>G	ENSP00000405470.1:n.*2102A>G
ENST00000634411.1:c.*236A>G	ENSP00000489135.1:n.*236A>G
ENST00000634664.1:n.859A>G
ENST00000635534.1:c.*236A>G	ENSP00000489229.1:n.*236A>G
ENST00000703612.1:c.*236A>G	ENSP00000515396.1:n.*236A>G
ENST00000703616.1:c.*236A>G	ENSP00000515400.1:n.*236A>G
XM_011516706.1:c.*236A>G	XP_011515008.1:n.*236A>G
XM_017012801.2:c.*236A>G	XP_016868290.1:n.*236A>G