Canonical Allele Identifier: CA931867474
Gene: FGF8 HGNC NCBI

Linked Data

dbSNP Id: rs2065030535

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101771757del , CM000672.2:g.101771757del GRCh38
NC_000010.10:g.103531514del , CM000672.1:g.103531514del GRCh37
NC_000010.9:g.103521504del NCBI36
NG_007151.1:g.9317del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.338-185del MANE Select ENSP00000321797.2:n.338-185del
ENST00000618991.5:c.26-185del ENSP00000484420.1:n.26-185del
ENST00000344255.8:c.305-185del ENSP00000340039.3:n.305-185del
ENST00000320185.6:c.338-185del ENSP00000321797.2:n.338-185del
ENST00000344255.7:c.305-185del ENSP00000340039.3:n.305-185del
ENST00000346714.7:c.218-185del ENSP00000344306.3:n.218-185del
ENST00000347978.2:c.251-185del ENSP00000321945.2:n.251-185del
ENST00000469792.6:c.*302-185del ENSP00000473299.1:n.*302-185del
ENST00000485728.1:n.214-185del
ENST00000618991.4:c.26-185del ENSP00000484420.1:n.26-185del
NM_001206389.1:c.26-185del NP_001193318.1:n.26-185del
NM_006119.4:c.251-185del NP_006110.1:n.251-185del
NM_033163.3:c.338-185del NP_149353.1:n.338-185del
NM_033164.3:c.305-185del NP_149354.1:n.305-185del
NM_033165.3:c.218-185del NP_149355.1:n.218-185del
XM_011539509.1:c.260-185del XP_011537811.1:n.260-185del
XR_946252.2:n.559del
XR_946253.2:n.557del
NM_006119.5:c.251-185del NP_006110.1:n.251-185del
NM_033163.4:c.338-185del NP_149353.1:n.338-185del
NM_033164.4:c.305-185del NP_149354.1:n.305-185del
NM_033165.4:c.218-185del NP_149355.1:n.218-185del
NM_001206389.2:c.26-185del NP_001193318.1:n.26-185del
NM_006119.6:c.251-185del NP_006110.1:n.251-185del
NM_033163.5:c.338-185del MANE Select NP_149353.1:n.338-185del
NM_033165.5:c.218-185del NP_149355.1:n.218-185del