Canonical Allele Identifier: CA377836321
Gene: FGF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101774770T>A , CM000672.2:g.101774770T>A GRCh38
NC_000010.10:g.103534527T>A , CM000672.1:g.103534527T>A GRCh37
NC_000010.9:g.103524517T>A NCBI36
NG_007151.1:g.6301A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.299A>T MANE Select ENSP00000321797.2:p.Lys100Met
ENST00000618991.5:c.-14A>T ENSP00000484420.1:n.-14A>T
ENST00000344255.8:c.266A>T ENSP00000340039.3:p.Lys89Met
ENST00000320185.6:c.299A>T ENSP00000321797.2:p.Lys100Met
ENST00000344255.7:c.266A>T ENSP00000340039.3:p.Lys89Met
ENST00000346714.7:c.179A>T ENSP00000344306.3:p.Lys60Met
ENST00000347978.2:c.212A>T ENSP00000321945.2:p.Lys71Met
ENST00000469792.6:c.*263A>T ENSP00000473299.1:n.*263A>T
ENST00000485728.1:n.175A>T
ENST00000618991.4:c.-14A>T ENSP00000484420.1:n.-14A>T
NM_001206389.1:c.-14A>T NP_001193318.1:n.-14A>T
NM_006119.4:c.212A>T NP_006110.1:p.Lys71Met
NM_033163.3:c.299A>T NP_149353.1:p.Lys100Met
NM_033164.3:c.266A>T NP_149354.1:p.Lys89Met
NM_033165.3:c.179A>T NP_149355.1:p.Lys60Met
XM_011539509.1:c.221A>T XP_011537811.1:p.Lys74Met
NM_006119.5:c.212A>T NP_006110.1:p.Lys71Met
NM_033163.4:c.299A>T NP_149353.1:p.Lys100Met
NM_033164.4:c.266A>T NP_149354.1:p.Lys89Met
NM_033165.4:c.179A>T NP_149355.1:p.Lys60Met
NM_001206389.2:c.-14A>T NP_001193318.1:n.-14A>T
NM_006119.6:c.212A>T NP_006110.1:p.Lys71Met
NM_033163.5:c.299A>T MANE Select NP_149353.1:p.Lys100Met
NM_033165.5:c.179A>T NP_149355.1:p.Lys60Met