Canonical Allele Identifier: CA1932376700

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774824G= , CM000672.2:g.101774824G=	GRCh38
NC_000010.10:g.103534581G= , CM000672.1:g.103534581G=	GRCh37
NC_000010.9:g.103524571G=	NCBI36
NG_007151.1:g.6247C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.245C= MANE Select	ENSP00000321797.2:p.Thr82=
ENST00000618991.5:c.-68C=	ENSP00000484420.1:n.-68C=
ENST00000344255.8:c.212C=	ENSP00000340039.3:p.Thr71=
ENST00000320185.6:c.245C=	ENSP00000321797.2:p.Thr82=
ENST00000344255.7:c.212C=	ENSP00000340039.3:p.Thr71=
ENST00000346714.7:c.125C=	ENSP00000344306.3:p.Thr42=
ENST00000347978.2:c.158C=	ENSP00000321945.2:p.Thr53=
ENST00000469792.6:c.*209C=	ENSP00000473299.1:n.*209C=
ENST00000485728.1:n.121C=
ENST00000618991.4:c.-68C=	ENSP00000484420.1:n.-68C=
NM_001206389.1:c.-68C=	NP_001193318.1:n.-68C=
NM_006119.4:c.158C=	NP_006110.1:p.Thr53=
NM_033163.3:c.245C=	NP_149353.1:p.Thr82=
NM_033164.3:c.212C=	NP_149354.1:p.Thr71=
NM_033165.3:c.125C=	NP_149355.1:p.Thr42=
XM_011539509.1:c.167C=	XP_011537811.1:p.Thr56=
NM_006119.5:c.158C=	NP_006110.1:p.Thr53=
NM_033163.4:c.245C=	NP_149353.1:p.Thr82=
NM_033164.4:c.212C=	NP_149354.1:p.Thr71=
NM_033165.4:c.125C=	NP_149355.1:p.Thr42=
NM_001206389.2:c.-68C=	NP_001193318.1:n.-68C=
NM_006119.6:c.158C=	NP_006110.1:p.Thr53=
NM_033163.5:c.245C= MANE Select	NP_149353.1:p.Thr82=
NM_033165.5:c.125C=	NP_149355.1:p.Thr42=