Canonical Allele Identifier: CA1932376631
Gene: FGF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101774785T= , CM000672.2:g.101774785T= GRCh38
NC_000010.10:g.103534542T= , CM000672.1:g.103534542T= GRCh37
NC_000010.9:g.103524532T= NCBI36
NG_007151.1:g.6286A=

Transcript Alleles

HGVS Amino-acid change
ENST00000320185.7:c.284A= MANE Select ENSP00000321797.2:p.Gln95=
ENST00000618991.5:c.-29A= ENSP00000484420.1:n.-29A=
ENST00000344255.8:c.251A= ENSP00000340039.3:p.Gln84=
ENST00000320185.6:c.284A= ENSP00000321797.2:p.Gln95=
ENST00000344255.7:c.251A= ENSP00000340039.3:p.Gln84=
ENST00000346714.7:c.164A= ENSP00000344306.3:p.Gln55=
ENST00000347978.2:c.197A= ENSP00000321945.2:p.Gln66=
ENST00000469792.6:c.*248A= ENSP00000473299.1:n.*248A=
ENST00000485728.1:n.160A=
ENST00000618991.4:c.-29A= ENSP00000484420.1:n.-29A=
NM_001206389.1:c.-29A= NP_001193318.1:n.-29A=
NM_006119.4:c.197A= NP_006110.1:p.Gln66=
NM_033163.3:c.284A= NP_149353.1:p.Gln95=
NM_033164.3:c.251A= NP_149354.1:p.Gln84=
NM_033165.3:c.164A= NP_149355.1:p.Gln55=
XM_011539509.1:c.206A= XP_011537811.1:p.Gln69=
NM_006119.5:c.197A= NP_006110.1:p.Gln66=
NM_033163.4:c.284A= NP_149353.1:p.Gln95=
NM_033164.4:c.251A= NP_149354.1:p.Gln84=
NM_033165.4:c.164A= NP_149355.1:p.Gln55=
NM_001206389.2:c.-29A= NP_001193318.1:n.-29A=
NM_006119.6:c.197A= NP_006110.1:p.Gln66=
NM_033163.5:c.284A= MANE Select NP_149353.1:p.Gln95=
NM_033165.5:c.164A= NP_149355.1:p.Gln55=