Canonical Allele Identifier: CA377834944
Gene: FGF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101771566T>G , CM000672.2:g.101771566T>G GRCh38
NC_000010.10:g.103531323T>G , CM000672.1:g.103531323T>G GRCh37
NC_000010.9:g.103521313T>G NCBI36
NG_007151.1:g.9505A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.341A>C MANE Select ENSP00000321797.2:p.Lys114Thr
ENST00000618991.5:c.29A>C ENSP00000484420.1:p.Lys10Thr
ENST00000344255.8:c.308A>C ENSP00000340039.3:p.Lys103Thr
ENST00000320185.6:c.341A>C ENSP00000321797.2:p.Lys114Thr
ENST00000344255.7:c.308A>C ENSP00000340039.3:p.Lys103Thr
ENST00000346714.7:c.221A>C ENSP00000344306.3:p.Lys74Thr
ENST00000347978.2:c.254A>C ENSP00000321945.2:p.Lys85Thr
ENST00000469792.6:c.*305A>C ENSP00000473299.1:n.*305A>C
ENST00000485728.1:n.217A>C
ENST00000618991.4:c.29A>C ENSP00000484420.1:p.Lys10Thr
NM_001206389.1:c.29A>C NP_001193318.1:p.Lys10Thr
NM_006119.4:c.254A>C NP_006110.1:p.Lys85Thr
NM_033163.3:c.341A>C NP_149353.1:p.Lys114Thr
NM_033164.3:c.308A>C NP_149354.1:p.Lys103Thr
NM_033165.3:c.221A>C NP_149355.1:p.Lys74Thr
XM_011539509.1:c.263A>C XP_011537811.1:p.Lys88Thr
XR_946251.1:n.347T>G
XR_946252.1:n.278T>G
XR_946253.1:n.276T>G
XR_946252.2:n.368T>G
XR_946253.2:n.366T>G
NM_006119.5:c.254A>C NP_006110.1:p.Lys85Thr
NM_033163.4:c.341A>C NP_149353.1:p.Lys114Thr
NM_033164.4:c.308A>C NP_149354.1:p.Lys103Thr
NM_033165.4:c.221A>C NP_149355.1:p.Lys74Thr
NM_001206389.2:c.29A>C NP_001193318.1:p.Lys10Thr
NM_006119.6:c.254A>C NP_006110.1:p.Lys85Thr
NM_033163.5:c.341A>C MANE Select NP_149353.1:p.Lys114Thr
NM_033165.5:c.221A>C NP_149355.1:p.Lys74Thr