Canonical Allele Identifier: CA1932376713

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774829G= , CM000672.2:g.101774829G=	GRCh38
NC_000010.10:g.103534586G= , CM000672.1:g.103534586G=	GRCh37
NC_000010.9:g.103524576G=	NCBI36
NG_007151.1:g.6242C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.240C= MANE Select	ENSP00000321797.2:p.Ile80=
ENST00000618991.5:c.-73C=	ENSP00000484420.1:n.-73C=
ENST00000344255.8:c.207C=	ENSP00000340039.3:p.Ile69=
ENST00000320185.6:c.240C=	ENSP00000321797.2:p.Ile80=
ENST00000344255.7:c.207C=	ENSP00000340039.3:p.Ile69=
ENST00000346714.7:c.120C=	ENSP00000344306.3:p.Ile40=
ENST00000347978.2:c.153C=	ENSP00000321945.2:p.Ile51=
ENST00000469792.6:c.*204C=	ENSP00000473299.1:n.*204C=
ENST00000485728.1:n.116C=
ENST00000618991.4:c.-73C=	ENSP00000484420.1:n.-73C=
NM_001206389.1:c.-73C=	NP_001193318.1:n.-73C=
NM_006119.4:c.153C=	NP_006110.1:p.Ile51=
NM_033163.3:c.240C=	NP_149353.1:p.Ile80=
NM_033164.3:c.207C=	NP_149354.1:p.Ile69=
NM_033165.3:c.120C=	NP_149355.1:p.Ile40=
XM_011539509.1:c.162C=	XP_011537811.1:p.Ile54=
NM_006119.5:c.153C=	NP_006110.1:p.Ile51=
NM_033163.4:c.240C=	NP_149353.1:p.Ile80=
NM_033164.4:c.207C=	NP_149354.1:p.Ile69=
NM_033165.4:c.120C=	NP_149355.1:p.Ile40=
NM_001206389.2:c.-73C=	NP_001193318.1:n.-73C=
NM_006119.6:c.153C=	NP_006110.1:p.Ile51=
NM_033163.5:c.240C= MANE Select	NP_149353.1:p.Ile80=
NM_033165.5:c.120C=	NP_149355.1:p.Ile40=