Canonical Allele Identifier: CA1932376741

Gene: FGF8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101774833A= , CM000672.2:g.101774833A=	GRCh38
NC_000010.10:g.103534590A= , CM000672.1:g.103534590A=	GRCh37
NC_000010.9:g.103524580A=	NCBI36
NG_007151.1:g.6238T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320185.7:c.236T= MANE Select	ENSP00000321797.2:p.Leu79=
ENST00000618991.5:c.-77T=	ENSP00000484420.1:n.-77T=
ENST00000344255.8:c.203T=	ENSP00000340039.3:p.Leu68=
ENST00000320185.6:c.236T=	ENSP00000321797.2:p.Leu79=
ENST00000344255.7:c.203T=	ENSP00000340039.3:p.Leu68=
ENST00000346714.7:c.116T=	ENSP00000344306.3:p.Leu39=
ENST00000347978.2:c.149T=	ENSP00000321945.2:p.Leu50=
ENST00000469792.6:c.*200T=	ENSP00000473299.1:n.*200T=
ENST00000485728.1:n.112T=
ENST00000618991.4:c.-77T=	ENSP00000484420.1:n.-77T=
NM_001206389.1:c.-77T=	NP_001193318.1:n.-77T=
NM_006119.4:c.149T=	NP_006110.1:p.Leu50=
NM_033163.3:c.236T=	NP_149353.1:p.Leu79=
NM_033164.3:c.203T=	NP_149354.1:p.Leu68=
NM_033165.3:c.116T=	NP_149355.1:p.Leu39=
XM_011539509.1:c.158T=	XP_011537811.1:p.Leu53=
NM_006119.5:c.149T=	NP_006110.1:p.Leu50=
NM_033163.4:c.236T=	NP_149353.1:p.Leu79=
NM_033164.4:c.203T=	NP_149354.1:p.Leu68=
NM_033165.4:c.116T=	NP_149355.1:p.Leu39=
NM_001206389.2:c.-77T=	NP_001193318.1:n.-77T=
NM_006119.6:c.149T=	NP_006110.1:p.Leu50=
NM_033163.5:c.236T= MANE Select	NP_149353.1:p.Leu79=
NM_033165.5:c.116T=	NP_149355.1:p.Leu39=