Canonical Allele Identifier: CA1932376626

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774783C= , CM000672.2:g.101774783C=	GRCh38
NC_000010.10:g.103534540C= , CM000672.1:g.103534540C=	GRCh37
NC_000010.9:g.103524530C=	NCBI36
NG_007151.1:g.6288G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.286G= MANE Select	ENSP00000321797.2:p.Val96=
ENST00000618991.5:c.-27G=	ENSP00000484420.1:n.-27G=
ENST00000344255.8:c.253G=	ENSP00000340039.3:p.Val85=
ENST00000320185.6:c.286G=	ENSP00000321797.2:p.Val96=
ENST00000344255.7:c.253G=	ENSP00000340039.3:p.Val85=
ENST00000346714.7:c.166G=	ENSP00000344306.3:p.Val56=
ENST00000347978.2:c.199G=	ENSP00000321945.2:p.Val67=
ENST00000469792.6:c.*250G=	ENSP00000473299.1:n.*250G=
ENST00000485728.1:n.162G=
ENST00000618991.4:c.-27G=	ENSP00000484420.1:n.-27G=
NM_001206389.1:c.-27G=	NP_001193318.1:n.-27G=
NM_006119.4:c.199G=	NP_006110.1:p.Val67=
NM_033163.3:c.286G=	NP_149353.1:p.Val96=
NM_033164.3:c.253G=	NP_149354.1:p.Val85=
NM_033165.3:c.166G=	NP_149355.1:p.Val56=
XM_011539509.1:c.208G=	XP_011537811.1:p.Val70=
NM_006119.5:c.199G=	NP_006110.1:p.Val67=
NM_033163.4:c.286G=	NP_149353.1:p.Val96=
NM_033164.4:c.253G=	NP_149354.1:p.Val85=
NM_033165.4:c.166G=	NP_149355.1:p.Val56=
NM_001206389.2:c.-27G=	NP_001193318.1:n.-27G=
NM_006119.6:c.199G=	NP_006110.1:p.Val67=
NM_033163.5:c.286G= MANE Select	NP_149353.1:p.Val96=
NM_033165.5:c.166G=	NP_149355.1:p.Val56=