Canonical Allele Identifier: CA377836774
Gene: FGF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101774812T>A , CM000672.2:g.101774812T>A GRCh38
NC_000010.10:g.103534569T>A , CM000672.1:g.103534569T>A GRCh37
NC_000010.9:g.103524559T>A NCBI36
NG_007151.1:g.6259A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.257A>T MANE Select ENSP00000321797.2:p.Tyr86Phe
ENST00000618991.5:c.-56A>T ENSP00000484420.1:n.-56A>T
ENST00000344255.8:c.224A>T ENSP00000340039.3:p.Tyr75Phe
ENST00000320185.6:c.257A>T ENSP00000321797.2:p.Tyr86Phe
ENST00000344255.7:c.224A>T ENSP00000340039.3:p.Tyr75Phe
ENST00000346714.7:c.137A>T ENSP00000344306.3:p.Tyr46Phe
ENST00000347978.2:c.170A>T ENSP00000321945.2:p.Tyr57Phe
ENST00000469792.6:c.*221A>T ENSP00000473299.1:n.*221A>T
ENST00000485728.1:n.133A>T
ENST00000618991.4:c.-56A>T ENSP00000484420.1:n.-56A>T
NM_001206389.1:c.-56A>T NP_001193318.1:n.-56A>T
NM_006119.4:c.170A>T NP_006110.1:p.Tyr57Phe
NM_033163.3:c.257A>T NP_149353.1:p.Tyr86Phe
NM_033164.3:c.224A>T NP_149354.1:p.Tyr75Phe
NM_033165.3:c.137A>T NP_149355.1:p.Tyr46Phe
XM_011539509.1:c.179A>T XP_011537811.1:p.Tyr60Phe
NM_006119.5:c.170A>T NP_006110.1:p.Tyr57Phe
NM_033163.4:c.257A>T NP_149353.1:p.Tyr86Phe
NM_033164.4:c.224A>T NP_149354.1:p.Tyr75Phe
NM_033165.4:c.137A>T NP_149355.1:p.Tyr46Phe
NM_001206389.2:c.-56A>T NP_001193318.1:n.-56A>T
NM_006119.6:c.170A>T NP_006110.1:p.Tyr57Phe
NM_033163.5:c.257A>T MANE Select NP_149353.1:p.Tyr86Phe
NM_033165.5:c.137A>T NP_149355.1:p.Tyr46Phe