Canonical Allele Identifier: CA1932376759
Gene: FGF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101774844G= , CM000672.2:g.101774844G= GRCh38
NC_000010.10:g.103534601G= , CM000672.1:g.103534601G= GRCh37
NC_000010.9:g.103524591G= NCBI36
NG_007151.1:g.6227C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320185.7:c.225C= MANE Select ENSP00000321797.2:p.Leu75=
ENST00000618991.5:c.-88C= ENSP00000484420.1:n.-88C=
ENST00000344255.8:c.192C= ENSP00000340039.3:p.Leu64=
ENST00000320185.6:c.225C= ENSP00000321797.2:p.Leu75=
ENST00000344255.7:c.192C= ENSP00000340039.3:p.Leu64=
ENST00000346714.7:c.105C= ENSP00000344306.3:p.Leu35=
ENST00000347978.2:c.138C= ENSP00000321945.2:p.Leu46=
ENST00000469792.6:c.*189C= ENSP00000473299.1:n.*189C=
ENST00000485728.1:n.101C=
ENST00000618991.4:c.-88C= ENSP00000484420.1:n.-88C=
NM_001206389.1:c.-88C= NP_001193318.1:n.-88C=
NM_006119.4:c.138C= NP_006110.1:p.Leu46=
NM_033163.3:c.225C= NP_149353.1:p.Leu75=
NM_033164.3:c.192C= NP_149354.1:p.Leu64=
NM_033165.3:c.105C= NP_149355.1:p.Leu35=
XM_011539509.1:c.147C= XP_011537811.1:p.Leu49=
NM_006119.5:c.138C= NP_006110.1:p.Leu46=
NM_033163.4:c.225C= NP_149353.1:p.Leu75=
NM_033164.4:c.192C= NP_149354.1:p.Leu64=
NM_033165.4:c.105C= NP_149355.1:p.Leu35=
NM_001206389.2:c.-88C= NP_001193318.1:n.-88C=
NM_006119.6:c.138C= NP_006110.1:p.Leu46=
NM_033163.5:c.225C= MANE Select NP_149353.1:p.Leu75=
NM_033165.5:c.105C= NP_149355.1:p.Leu35=