Canonical Allele Identifier: CA377836194
Gene: FGF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101774749T>G , CM000672.2:g.101774749T>G GRCh38
NC_000010.10:g.103534506T>G , CM000672.1:g.103534506T>G GRCh37
NC_000010.9:g.103524496T>G NCBI36
NG_007151.1:g.6322A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.320A>C MANE Select ENSP00000321797.2:p.Glu107Ala
ENST00000618991.5:c.8A>C ENSP00000484420.1:p.Glu3Ala
ENST00000344255.8:c.287A>C ENSP00000340039.3:p.Glu96Ala
ENST00000320185.6:c.320A>C ENSP00000321797.2:p.Glu107Ala
ENST00000344255.7:c.287A>C ENSP00000340039.3:p.Glu96Ala
ENST00000346714.7:c.200A>C ENSP00000344306.3:p.Glu67Ala
ENST00000347978.2:c.233A>C ENSP00000321945.2:p.Glu78Ala
ENST00000469792.6:c.*284A>C ENSP00000473299.1:n.*284A>C
ENST00000485728.1:n.196A>C
ENST00000618991.4:c.8A>C ENSP00000484420.1:p.Glu3Ala
NM_001206389.1:c.8A>C NP_001193318.1:p.Glu3Ala
NM_006119.4:c.233A>C NP_006110.1:p.Glu78Ala
NM_033163.3:c.320A>C NP_149353.1:p.Glu107Ala
NM_033164.3:c.287A>C NP_149354.1:p.Glu96Ala
NM_033165.3:c.200A>C NP_149355.1:p.Glu67Ala
XM_011539509.1:c.242A>C XP_011537811.1:p.Glu81Ala
NM_006119.5:c.233A>C NP_006110.1:p.Glu78Ala
NM_033163.4:c.320A>C NP_149353.1:p.Glu107Ala
NM_033164.4:c.287A>C NP_149354.1:p.Glu96Ala
NM_033165.4:c.200A>C NP_149355.1:p.Glu67Ala
NM_001206389.2:c.8A>C NP_001193318.1:p.Glu3Ala
NM_006119.6:c.233A>C NP_006110.1:p.Glu78Ala
NM_033163.5:c.320A>C MANE Select NP_149353.1:p.Glu107Ala
NM_033165.5:c.200A>C NP_149355.1:p.Glu67Ala