Canonical Allele Identifier: CA1932372668

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771562G= , CM000672.2:g.101771562G=	GRCh38
NC_000010.10:g.103531319G= , CM000672.1:g.103531319G=	GRCh37
NC_000010.9:g.103521309G=	NCBI36
NG_007151.1:g.9509C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.345C= MANE Select	ENSP00000321797.2:p.Leu115=
ENST00000618991.5:c.33C=	ENSP00000484420.1:p.Leu11=
ENST00000344255.8:c.312C=	ENSP00000340039.3:p.Leu104=
ENST00000320185.6:c.345C=	ENSP00000321797.2:p.Leu115=
ENST00000344255.7:c.312C=	ENSP00000340039.3:p.Leu104=
ENST00000346714.7:c.225C=	ENSP00000344306.3:p.Leu75=
ENST00000347978.2:c.258C=	ENSP00000321945.2:p.Leu86=
ENST00000469792.6:c.*309C=	ENSP00000473299.1:n.*309C=
ENST00000485728.1:n.221C=
ENST00000618991.4:c.33C=	ENSP00000484420.1:p.Leu11=
NM_001206389.1:c.33C=	NP_001193318.1:p.Leu11=
NM_006119.4:c.258C=	NP_006110.1:p.Leu86=
NM_033163.3:c.345C=	NP_149353.1:p.Leu115=
NM_033164.3:c.312C=	NP_149354.1:p.Leu104=
NM_033165.3:c.225C=	NP_149355.1:p.Leu75=
XM_011539509.1:c.267C=	XP_011537811.1:p.Leu89=
XR_946251.1:n.343G=
XR_946252.1:n.274G=
XR_946253.1:n.272G=
XR_946252.2:n.364G=
XR_946253.2:n.362G=
NM_006119.5:c.258C=	NP_006110.1:p.Leu86=
NM_033163.4:c.345C=	NP_149353.1:p.Leu115=
NM_033164.4:c.312C=	NP_149354.1:p.Leu104=
NM_033165.4:c.225C=	NP_149355.1:p.Leu75=
NM_001206389.2:c.33C=	NP_001193318.1:p.Leu11=
NM_006119.6:c.258C=	NP_006110.1:p.Leu86=
NM_033163.5:c.345C= MANE Select	NP_149353.1:p.Leu115=
NM_033165.5:c.225C=	NP_149355.1:p.Leu75=