Canonical Allele Identifier: CA1932372613

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771528G= , CM000672.2:g.101771528G=	GRCh38
NC_000010.10:g.103531285G= , CM000672.1:g.103531285G=	GRCh37
NC_000010.9:g.103521275G=	NCBI36
NG_007151.1:g.9543C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320185.7:c.379C= MANE Select	ENSP00000321797.2:p.Arg127=
ENST00000618991.5:c.67C=	ENSP00000484420.1:p.Arg23=
ENST00000344255.8:c.346C=	ENSP00000340039.3:p.Arg116=
ENST00000320185.6:c.379C=	ENSP00000321797.2:p.Arg127=
ENST00000344255.7:c.346C=	ENSP00000340039.3:p.Arg116=
ENST00000346714.7:c.259C=	ENSP00000344306.3:p.Arg87=
ENST00000347978.2:c.292C=	ENSP00000321945.2:p.Arg98=
ENST00000469792.6:c.*343C=	ENSP00000473299.1:n.*343C=
ENST00000485728.1:n.255C=
ENST00000618991.4:c.67C=	ENSP00000484420.1:p.Arg23=
NM_001206389.1:c.67C=	NP_001193318.1:p.Arg23=
NM_006119.4:c.292C=	NP_006110.1:p.Arg98=
NM_033163.3:c.379C=	NP_149353.1:p.Arg127=
NM_033164.3:c.346C=	NP_149354.1:p.Arg116=
NM_033165.3:c.259C=	NP_149355.1:p.Arg87=
XM_011539509.1:c.301C=	XP_011537811.1:p.Arg101=
XR_946251.1:n.309G=
XR_946252.1:n.240G=
XR_946253.1:n.238G=
XR_946252.2:n.330G=
XR_946253.2:n.328G=
NM_006119.5:c.292C=	NP_006110.1:p.Arg98=
NM_033163.4:c.379C=	NP_149353.1:p.Arg127=
NM_033164.4:c.346C=	NP_149354.1:p.Arg116=
NM_033165.4:c.259C=	NP_149355.1:p.Arg87=
NM_001206389.2:c.67C=	NP_001193318.1:p.Arg23=
NM_006119.6:c.292C=	NP_006110.1:p.Arg98=
NM_033163.5:c.379C= MANE Select	NP_149353.1:p.Arg127=
NM_033165.5:c.259C=	NP_149355.1:p.Arg87=