Canonical Allele Identifier: CA1932372632

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771532T= , CM000672.2:g.101771532T=	GRCh38
NC_000010.10:g.103531289T= , CM000672.1:g.103531289T=	GRCh37
NC_000010.9:g.103521279T=	NCBI36
NG_007151.1:g.9539A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.375A= MANE Select	ENSP00000321797.2:p.Arg125=
ENST00000618991.5:c.63A=	ENSP00000484420.1:p.Arg21=
ENST00000344255.8:c.342A=	ENSP00000340039.3:p.Arg114=
ENST00000320185.6:c.375A=	ENSP00000321797.2:p.Arg125=
ENST00000344255.7:c.342A=	ENSP00000340039.3:p.Arg114=
ENST00000346714.7:c.255A=	ENSP00000344306.3:p.Arg85=
ENST00000347978.2:c.288A=	ENSP00000321945.2:p.Arg96=
ENST00000469792.6:c.*339A=	ENSP00000473299.1:n.*339A=
ENST00000485728.1:n.251A=
ENST00000618991.4:c.63A=	ENSP00000484420.1:p.Arg21=
NM_001206389.1:c.63A=	NP_001193318.1:p.Arg21=
NM_006119.4:c.288A=	NP_006110.1:p.Arg96=
NM_033163.3:c.375A=	NP_149353.1:p.Arg125=
NM_033164.3:c.342A=	NP_149354.1:p.Arg114=
NM_033165.3:c.255A=	NP_149355.1:p.Arg85=
XM_011539509.1:c.297A=	XP_011537811.1:p.Arg99=
XR_946251.1:n.313T=
XR_946252.1:n.244T=
XR_946253.1:n.242T=
XR_946252.2:n.334T=
XR_946253.2:n.332T=
NM_006119.5:c.288A=	NP_006110.1:p.Arg96=
NM_033163.4:c.375A=	NP_149353.1:p.Arg125=
NM_033164.4:c.342A=	NP_149354.1:p.Arg114=
NM_033165.4:c.255A=	NP_149355.1:p.Arg85=
NM_001206389.2:c.63A=	NP_001193318.1:p.Arg21=
NM_006119.6:c.288A=	NP_006110.1:p.Arg96=
NM_033163.5:c.375A= MANE Select	NP_149353.1:p.Arg125=
NM_033165.5:c.255A=	NP_149355.1:p.Arg85=