Canonical Allele Identifier: CA1932377125
Gene: FGF8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101775088C= , CM000672.2:g.101775088C= GRCh38
NC_000010.10:g.103534845C= , CM000672.1:g.103534845C= GRCh37
NC_000010.9:g.103524835C= NCBI36
NG_007151.1:g.5983G=

Transcript Alleles

HGVS Amino-acid change
ENST00000320185.7:c.156+42G= MANE Select ENSP00000321797.2:n.156+42G=
ENST00000618991.5:c.-123-209G= ENSP00000484420.1:n.-123-209G=
ENST00000344255.8:c.156+42G= ENSP00000340039.3:n.156+42G=
ENST00000320185.6:c.156+42G= ENSP00000321797.2:n.156+42G=
ENST00000344255.7:c.156+42G= ENSP00000340039.3:n.156+42G=
ENST00000346714.7:c.70-209G= ENSP00000344306.3:n.70-209G=
ENST00000347978.2:c.70-176G= ENSP00000321945.2:n.70-176G=
ENST00000469792.6:c.*154-209G= ENSP00000473299.1:n.*154-209G=
ENST00000485728.1:n.33-176G=
ENST00000618991.4:c.-123-209G= ENSP00000484420.1:n.-123-209G=
NM_001206389.1:c.-123-209G= NP_001193318.1:n.-123-209G=
NM_006119.4:c.70-176G= NP_006110.1:n.70-176G=
NM_033163.3:c.156+42G= NP_149353.1:n.156+42G=
NM_033164.3:c.156+42G= NP_149354.1:n.156+42G=
NM_033165.3:c.70-209G= NP_149355.1:n.70-209G=
XM_011539509.1:c.79-176G= XP_011537811.1:n.79-176G=
NM_006119.5:c.70-176G= NP_006110.1:n.70-176G=
NM_033163.4:c.156+42G= NP_149353.1:n.156+42G=
NM_033164.4:c.156+42G= NP_149354.1:n.156+42G=
NM_033165.4:c.70-209G= NP_149355.1:n.70-209G=
NM_001206389.2:c.-123-209G= NP_001193318.1:n.-123-209G=
NM_006119.6:c.70-176G= NP_006110.1:n.70-176G=
NM_033163.5:c.156+42G= MANE Select NP_149353.1:n.156+42G=
NM_033165.5:c.70-209G= NP_149355.1:n.70-209G=