Canonical Allele Identifier: CA1932372658

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771556C= , CM000672.2:g.101771556C=	GRCh38
NC_000010.10:g.103531313C= , CM000672.1:g.103531313C=	GRCh37
NC_000010.9:g.103521303C=	NCBI36
NG_007151.1:g.9515G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.351G= MANE Select	ENSP00000321797.2:p.Val117=
ENST00000618991.5:c.39G=	ENSP00000484420.1:p.Val13=
ENST00000344255.8:c.318G=	ENSP00000340039.3:p.Val106=
ENST00000320185.6:c.351G=	ENSP00000321797.2:p.Val117=
ENST00000344255.7:c.318G=	ENSP00000340039.3:p.Val106=
ENST00000346714.7:c.231G=	ENSP00000344306.3:p.Val77=
ENST00000347978.2:c.264G=	ENSP00000321945.2:p.Val88=
ENST00000469792.6:c.*315G=	ENSP00000473299.1:n.*315G=
ENST00000485728.1:n.227G=
ENST00000618991.4:c.39G=	ENSP00000484420.1:p.Val13=
NM_001206389.1:c.39G=	NP_001193318.1:p.Val13=
NM_006119.4:c.264G=	NP_006110.1:p.Val88=
NM_033163.3:c.351G=	NP_149353.1:p.Val117=
NM_033164.3:c.318G=	NP_149354.1:p.Val106=
NM_033165.3:c.231G=	NP_149355.1:p.Val77=
XM_011539509.1:c.273G=	XP_011537811.1:p.Val91=
XR_946251.1:n.337C=
XR_946252.1:n.268C=
XR_946253.1:n.266C=
XR_946252.2:n.358C=
XR_946253.2:n.356C=
NM_006119.5:c.264G=	NP_006110.1:p.Val88=
NM_033163.4:c.351G=	NP_149353.1:p.Val117=
NM_033164.4:c.318G=	NP_149354.1:p.Val106=
NM_033165.4:c.231G=	NP_149355.1:p.Val77=
NM_001206389.2:c.39G=	NP_001193318.1:p.Val13=
NM_006119.6:c.264G=	NP_006110.1:p.Val88=
NM_033163.5:c.351G= MANE Select	NP_149353.1:p.Val117=
NM_033165.5:c.231G=	NP_149355.1:p.Val77=