Canonical Allele Identifier: CA2610620503
Gene: FGF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101775043_101775044del , CM000672.2:g.101775043_101775044del GRCh38
NC_000010.10:g.103534800_103534801del , CM000672.1:g.103534800_103534801del GRCh37
NC_000010.9:g.103524790_103524791del NCBI36
NG_007151.1:g.6027_6028del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.156+86_156+87del MANE Select ENSP00000321797.2:n.156+86_156+87del
ENST00000618991.5:c.-123-165_-123-164del ENSP00000484420.1:n.-123-165_-123-164del
ENST00000344255.8:c.156+86_156+87del ENSP00000340039.3:n.156+86_156+87del
ENST00000320185.6:c.156+86_156+87del ENSP00000321797.2:n.156+86_156+87del
ENST00000344255.7:c.156+86_156+87del ENSP00000340039.3:n.156+86_156+87del
ENST00000346714.7:c.70-165_70-164del ENSP00000344306.3:n.70-165_70-164del
ENST00000347978.2:c.70-132_70-131del ENSP00000321945.2:n.70-132_70-131del
ENST00000469792.6:c.*154-165_*154-164del ENSP00000473299.1:n.*154-165_*154-164del
ENST00000485728.1:n.33-132_33-131del
ENST00000618991.4:c.-123-165_-123-164del ENSP00000484420.1:n.-123-165_-123-164del
NM_001206389.1:c.-123-165_-123-164del NP_001193318.1:n.-123-165_-123-164del
NM_006119.4:c.70-132_70-131del NP_006110.1:n.70-132_70-131del
NM_033163.3:c.156+86_156+87del NP_149353.1:n.156+86_156+87del
NM_033164.3:c.156+86_156+87del NP_149354.1:n.156+86_156+87del
NM_033165.3:c.70-165_70-164del NP_149355.1:n.70-165_70-164del
XM_011539509.1:c.79-132_79-131del XP_011537811.1:n.79-132_79-131del
NM_006119.5:c.70-132_70-131del NP_006110.1:n.70-132_70-131del
NM_033163.4:c.156+86_156+87del NP_149353.1:n.156+86_156+87del
NM_033164.4:c.156+86_156+87del NP_149354.1:n.156+86_156+87del
NM_033165.4:c.70-165_70-164del NP_149355.1:n.70-165_70-164del
NM_001206389.2:c.-123-165_-123-164del NP_001193318.1:n.-123-165_-123-164del
NM_006119.6:c.70-132_70-131del NP_006110.1:n.70-132_70-131del
NM_033163.5:c.156+86_156+87del MANE Select NP_149353.1:n.156+86_156+87del
NM_033165.5:c.70-165_70-164del NP_149355.1:n.70-165_70-164del