Canonical Allele Identifier: CA1932372643

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771547G= , CM000672.2:g.101771547G=	GRCh38
NC_000010.10:g.103531304G= , CM000672.1:g.103531304G=	GRCh37
NC_000010.9:g.103521294G=	NCBI36
NG_007151.1:g.9524C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.360C= MANE Select	ENSP00000321797.2:p.Asp120=
ENST00000618991.5:c.48C=	ENSP00000484420.1:p.Asp16=
ENST00000344255.8:c.327C=	ENSP00000340039.3:p.Asp109=
ENST00000320185.6:c.360C=	ENSP00000321797.2:p.Asp120=
ENST00000344255.7:c.327C=	ENSP00000340039.3:p.Asp109=
ENST00000346714.7:c.240C=	ENSP00000344306.3:p.Asp80=
ENST00000347978.2:c.273C=	ENSP00000321945.2:p.Asp91=
ENST00000469792.6:c.*324C=	ENSP00000473299.1:n.*324C=
ENST00000485728.1:n.236C=
ENST00000618991.4:c.48C=	ENSP00000484420.1:p.Asp16=
NM_001206389.1:c.48C=	NP_001193318.1:p.Asp16=
NM_006119.4:c.273C=	NP_006110.1:p.Asp91=
NM_033163.3:c.360C=	NP_149353.1:p.Asp120=
NM_033164.3:c.327C=	NP_149354.1:p.Asp109=
NM_033165.3:c.240C=	NP_149355.1:p.Asp80=
XM_011539509.1:c.282C=	XP_011537811.1:p.Asp94=
XR_946251.1:n.328G=
XR_946252.1:n.259G=
XR_946253.1:n.257G=
XR_946252.2:n.349G=
XR_946253.2:n.347G=
NM_006119.5:c.273C=	NP_006110.1:p.Asp91=
NM_033163.4:c.360C=	NP_149353.1:p.Asp120=
NM_033164.4:c.327C=	NP_149354.1:p.Asp109=
NM_033165.4:c.240C=	NP_149355.1:p.Asp80=
NM_001206389.2:c.48C=	NP_001193318.1:p.Asp16=
NM_006119.6:c.273C=	NP_006110.1:p.Asp91=
NM_033163.5:c.360C= MANE Select	NP_149353.1:p.Asp120=
NM_033165.5:c.240C=	NP_149355.1:p.Asp80=