Canonical Allele Identifier: CA2610620010
Gene: FGF8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101771667del , CM000672.2:g.101771667del GRCh38
NC_000010.10:g.103531424del , CM000672.1:g.103531424del GRCh37
NC_000010.9:g.103521414del NCBI36
NG_007151.1:g.9405del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320185.7:c.338-97del MANE Select ENSP00000321797.2:n.338-97del
ENST00000618991.5:c.26-97del ENSP00000484420.1:n.26-97del
ENST00000344255.8:c.305-97del ENSP00000340039.3:n.305-97del
ENST00000320185.6:c.338-97del ENSP00000321797.2:n.338-97del
ENST00000344255.7:c.305-97del ENSP00000340039.3:n.305-97del
ENST00000346714.7:c.218-97del ENSP00000344306.3:n.218-97del
ENST00000347978.2:c.251-97del ENSP00000321945.2:n.251-97del
ENST00000469792.6:c.*302-97del ENSP00000473299.1:n.*302-97del
ENST00000485728.1:n.214-97del
ENST00000618991.4:c.26-97del ENSP00000484420.1:n.26-97del
NM_001206389.1:c.26-97del NP_001193318.1:n.26-97del
NM_006119.4:c.251-97del NP_006110.1:n.251-97del
NM_033163.3:c.338-97del NP_149353.1:n.338-97del
NM_033164.3:c.305-97del NP_149354.1:n.305-97del
NM_033165.3:c.218-97del NP_149355.1:n.218-97del
XM_011539509.1:c.260-97del XP_011537811.1:n.260-97del
XR_946252.2:n.469del
XR_946253.2:n.467del
NM_006119.5:c.251-97del NP_006110.1:n.251-97del
NM_033163.4:c.338-97del NP_149353.1:n.338-97del
NM_033164.4:c.305-97del NP_149354.1:n.305-97del
NM_033165.4:c.218-97del NP_149355.1:n.218-97del
NM_001206389.2:c.26-97del NP_001193318.1:n.26-97del
NM_006119.6:c.251-97del NP_006110.1:n.251-97del
NM_033163.5:c.338-97del MANE Select NP_149353.1:n.338-97del
NM_033165.5:c.218-97del NP_149355.1:n.218-97del