Canonical Allele Identifier: CA1932376669

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774808G= , CM000672.2:g.101774808G=	GRCh38
NC_000010.10:g.103534565G= , CM000672.1:g.103534565G=	GRCh37
NC_000010.9:g.103524555G=	NCBI36
NG_007151.1:g.6263C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.261C= MANE Select	ENSP00000321797.2:p.Ser87=
ENST00000618991.5:c.-52C=	ENSP00000484420.1:n.-52C=
ENST00000344255.8:c.228C=	ENSP00000340039.3:p.Ser76=
ENST00000320185.6:c.261C=	ENSP00000321797.2:p.Ser87=
ENST00000344255.7:c.228C=	ENSP00000340039.3:p.Ser76=
ENST00000346714.7:c.141C=	ENSP00000344306.3:p.Ser47=
ENST00000347978.2:c.174C=	ENSP00000321945.2:p.Ser58=
ENST00000469792.6:c.*225C=	ENSP00000473299.1:n.*225C=
ENST00000485728.1:n.137C=
ENST00000618991.4:c.-52C=	ENSP00000484420.1:n.-52C=
NM_001206389.1:c.-52C=	NP_001193318.1:n.-52C=
NM_006119.4:c.174C=	NP_006110.1:p.Ser58=
NM_033163.3:c.261C=	NP_149353.1:p.Ser87=
NM_033164.3:c.228C=	NP_149354.1:p.Ser76=
NM_033165.3:c.141C=	NP_149355.1:p.Ser47=
XM_011539509.1:c.183C=	XP_011537811.1:p.Ser61=
NM_006119.5:c.174C=	NP_006110.1:p.Ser58=
NM_033163.4:c.261C=	NP_149353.1:p.Ser87=
NM_033164.4:c.228C=	NP_149354.1:p.Ser76=
NM_033165.4:c.141C=	NP_149355.1:p.Ser47=
NM_001206389.2:c.-52C=	NP_001193318.1:n.-52C=
NM_006119.6:c.174C=	NP_006110.1:p.Ser58=
NM_033163.5:c.261C= MANE Select	NP_149353.1:p.Ser87=
NM_033165.5:c.141C=	NP_149355.1:p.Ser47=