Canonical Allele Identifier: CA1932376755
Gene: FGF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101774841G= , CM000672.2:g.101774841G= GRCh38
NC_000010.10:g.103534598G= , CM000672.1:g.103534598G= GRCh37
NC_000010.9:g.103524588G= NCBI36
NG_007151.1:g.6230C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320185.7:c.228C= MANE Select ENSP00000321797.2:p.Ser76=
ENST00000618991.5:c.-85C= ENSP00000484420.1:n.-85C=
ENST00000344255.8:c.195C= ENSP00000340039.3:p.Ser65=
ENST00000320185.6:c.228C= ENSP00000321797.2:p.Ser76=
ENST00000344255.7:c.195C= ENSP00000340039.3:p.Ser65=
ENST00000346714.7:c.108C= ENSP00000344306.3:p.Ser36=
ENST00000347978.2:c.141C= ENSP00000321945.2:p.Ser47=
ENST00000469792.6:c.*192C= ENSP00000473299.1:n.*192C=
ENST00000485728.1:n.104C=
ENST00000618991.4:c.-85C= ENSP00000484420.1:n.-85C=
NM_001206389.1:c.-85C= NP_001193318.1:n.-85C=
NM_006119.4:c.141C= NP_006110.1:p.Ser47=
NM_033163.3:c.228C= NP_149353.1:p.Ser76=
NM_033164.3:c.195C= NP_149354.1:p.Ser65=
NM_033165.3:c.108C= NP_149355.1:p.Ser36=
XM_011539509.1:c.150C= XP_011537811.1:p.Ser50=
NM_006119.5:c.141C= NP_006110.1:p.Ser47=
NM_033163.4:c.228C= NP_149353.1:p.Ser76=
NM_033164.4:c.195C= NP_149354.1:p.Ser65=
NM_033165.4:c.108C= NP_149355.1:p.Ser36=
NM_001206389.2:c.-85C= NP_001193318.1:n.-85C=
NM_006119.6:c.141C= NP_006110.1:p.Ser47=
NM_033163.5:c.228C= MANE Select NP_149353.1:p.Ser76=
NM_033165.5:c.108C= NP_149355.1:p.Ser36=