Canonical Allele Identifier: CA377836343
Gene: FGF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101774771T>G , CM000672.2:g.101774771T>G GRCh38
NC_000010.10:g.103534528T>G , CM000672.1:g.103534528T>G GRCh37
NC_000010.9:g.103524518T>G NCBI36
NG_007151.1:g.6300A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.298A>C MANE Select ENSP00000321797.2:p.Lys100Gln
ENST00000618991.5:c.-15A>C ENSP00000484420.1:n.-15A>C
ENST00000344255.8:c.265A>C ENSP00000340039.3:p.Lys89Gln
ENST00000320185.6:c.298A>C ENSP00000321797.2:p.Lys100Gln
ENST00000344255.7:c.265A>C ENSP00000340039.3:p.Lys89Gln
ENST00000346714.7:c.178A>C ENSP00000344306.3:p.Lys60Gln
ENST00000347978.2:c.211A>C ENSP00000321945.2:p.Lys71Gln
ENST00000469792.6:c.*262A>C ENSP00000473299.1:n.*262A>C
ENST00000485728.1:n.174A>C
ENST00000618991.4:c.-15A>C ENSP00000484420.1:n.-15A>C
NM_001206389.1:c.-15A>C NP_001193318.1:n.-15A>C
NM_006119.4:c.211A>C NP_006110.1:p.Lys71Gln
NM_033163.3:c.298A>C NP_149353.1:p.Lys100Gln
NM_033164.3:c.265A>C NP_149354.1:p.Lys89Gln
NM_033165.3:c.178A>C NP_149355.1:p.Lys60Gln
XM_011539509.1:c.220A>C XP_011537811.1:p.Lys74Gln
NM_006119.5:c.211A>C NP_006110.1:p.Lys71Gln
NM_033163.4:c.298A>C NP_149353.1:p.Lys100Gln
NM_033164.4:c.265A>C NP_149354.1:p.Lys89Gln
NM_033165.4:c.178A>C NP_149355.1:p.Lys60Gln
NM_001206389.2:c.-15A>C NP_001193318.1:n.-15A>C
NM_006119.6:c.211A>C NP_006110.1:p.Lys71Gln
NM_033163.5:c.298A>C MANE Select NP_149353.1:p.Lys100Gln
NM_033165.5:c.178A>C NP_149355.1:p.Lys60Gln