Canonical Allele Identifier: CA1932372630

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101771531C= , CM000672.2:g.101771531C=	GRCh38
NC_000010.10:g.103531288C= , CM000672.1:g.103531288C=	GRCh37
NC_000010.9:g.103521278C=	NCBI36
NG_007151.1:g.9540G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320185.7:c.376G= MANE Select	ENSP00000321797.2:p.Val126=
ENST00000618991.5:c.64G=	ENSP00000484420.1:p.Val22=
ENST00000344255.8:c.343G=	ENSP00000340039.3:p.Val115=
ENST00000320185.6:c.376G=	ENSP00000321797.2:p.Val126=
ENST00000344255.7:c.343G=	ENSP00000340039.3:p.Val115=
ENST00000346714.7:c.256G=	ENSP00000344306.3:p.Val86=
ENST00000347978.2:c.289G=	ENSP00000321945.2:p.Val97=
ENST00000469792.6:c.*340G=	ENSP00000473299.1:n.*340G=
ENST00000485728.1:n.252G=
ENST00000618991.4:c.64G=	ENSP00000484420.1:p.Val22=
NM_001206389.1:c.64G=	NP_001193318.1:p.Val22=
NM_006119.4:c.289G=	NP_006110.1:p.Val97=
NM_033163.3:c.376G=	NP_149353.1:p.Val126=
NM_033164.3:c.343G=	NP_149354.1:p.Val115=
NM_033165.3:c.256G=	NP_149355.1:p.Val86=
XM_011539509.1:c.298G=	XP_011537811.1:p.Val100=
XR_946251.1:n.312C=
XR_946252.1:n.243C=
XR_946253.1:n.241C=
XR_946252.2:n.333C=
XR_946253.2:n.331C=
NM_006119.5:c.289G=	NP_006110.1:p.Val97=
NM_033163.4:c.376G=	NP_149353.1:p.Val126=
NM_033164.4:c.343G=	NP_149354.1:p.Val115=
NM_033165.4:c.256G=	NP_149355.1:p.Val86=
NM_001206389.2:c.64G=	NP_001193318.1:p.Val22=
NM_006119.6:c.289G=	NP_006110.1:p.Val97=
NM_033163.5:c.376G= MANE Select	NP_149353.1:p.Val126=
NM_033165.5:c.256G=	NP_149355.1:p.Val86=