Canonical Allele Identifier: CA1735896018

Gene: FOXP2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.114349147G= , CM000669.2:g.114349147G=	GRCh38
NC_000007.13:g.113989202G= , CM000669.1:g.113989202G=	GRCh37
NC_000007.12:g.113776438G=	NCBI36
NG_007491.2:g.267838G=
NG_007491.3:g.267838G=

Transcript Alleles

HGVS	Amino-acid Change
NR_033766.1:n.393+61038G=
NR_033766.2:n.376+61038G=
ENST00000412402.5:c.-11+61038G=	ENSP00000405470.1:n.-11+61038G=
ENST00000440349.5:c.-11+61038G=	ENSP00000395552.1:n.-11+61038G=
ENST00000441290.6:c.-146-17358G=	ENSP00000416825.1:n.-146-17358G=
ENST00000495516.1:n.341+61038G=
ENST00000634411.1:c.-11+61038G=	ENSP00000489135.1:n.-11+61038G=
ENST00000634623.1:c.-11+61038G=	ENSP00000488944.1:n.-11+61038G=
ENST00000635109.1:c.-11+61038G=	ENSP00000489457.1:n.-11+61038G=
ENST00000635638.1:c.-11+61038G=	ENSP00000489073.1:n.-11+61038G=
ENST00000703612.1:c.-11+61038G=	ENSP00000515396.1:n.-11+61038G=
ENST00000703613.1:c.-11+61038G=	ENSP00000515397.1:n.-11+61038G=
ENST00000703614.1:c.-11+61038G=	ENSP00000515398.1:n.-11+61038G=
ENST00000703615.1:c.-11+61038G=	ENSP00000515399.1:n.-11+61038G=
ENST00000703616.1:c.-11+61038G=	ENSP00000515400.1:n.-11+61038G=
XM_011516706.1:c.-11+29077G=	XP_011515008.1:n.-11+29077G=
XM_017012801.2:c.-11+61038G=	XP_016868290.1:n.-11+61038G=