Canonical Allele Identifier: CA931868737
Gene: FGF8 HGNC NCBI

Linked Data

dbSNP Id: rs2065074044

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101775259del , CM000672.2:g.101775259del GRCh38
NC_000010.10:g.103535016del , CM000672.1:g.103535016del GRCh37
NC_000010.9:g.103525006del NCBI36
NG_007151.1:g.5815del

Transcript Alleles

HGVS Amino-acid change
ENST00000320185.7:c.70-40del MANE Select ENSP00000321797.2:n.70-40del
ENST00000618991.5:c.-123-377del ENSP00000484420.1:n.-123-377del
ENST00000344255.8:c.70-40del ENSP00000340039.3:n.70-40del
ENST00000320185.6:c.70-40del ENSP00000321797.2:n.70-40del
ENST00000344255.7:c.70-40del ENSP00000340039.3:n.70-40del
ENST00000346714.7:c.70-377del ENSP00000344306.3:n.70-377del
ENST00000347978.2:c.70-344del ENSP00000321945.2:n.70-344del
ENST00000469792.6:c.*153+286del ENSP00000473299.1:n.*153+286del
ENST00000485728.1:n.33-344del
ENST00000618991.4:c.-123-377del ENSP00000484420.1:n.-123-377del
NM_001206389.1:c.-123-377del NP_001193318.1:n.-123-377del
NM_006119.4:c.70-344del NP_006110.1:n.70-344del
NM_033163.3:c.70-40del NP_149353.1:n.70-40del
NM_033164.3:c.70-40del NP_149354.1:n.70-40del
NM_033165.3:c.70-377del NP_149355.1:n.70-377del
XM_011539509.1:c.79-344del XP_011537811.1:n.79-344del
NM_006119.5:c.70-344del NP_006110.1:n.70-344del
NM_033163.4:c.70-40del NP_149353.1:n.70-40del
NM_033164.4:c.70-40del NP_149354.1:n.70-40del
NM_033165.4:c.70-377del NP_149355.1:n.70-377del
NM_001206389.2:c.-123-377del NP_001193318.1:n.-123-377del
NM_006119.6:c.70-344del NP_006110.1:n.70-344del
NM_033163.5:c.70-40del MANE Select NP_149353.1:n.70-40del
NM_033165.5:c.70-377del NP_149355.1:n.70-377del