Canonical Allele Identifier: CA174665192
Gene: FZD3 HGNC NCBI

Linked Data

dbSNP Id: rs760598311

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28533490del , CM000670.2:g.28533490del GRCh38
NC_000008.10:g.28391007del , CM000670.1:g.28391007del GRCh37
NC_000008.9:g.28446926del NCBI36
NG_029723.1:g.44286del

Transcript Alleles

HGVS Amino-acid Change
ENST00000240093.8:c.1404+5326del MANE Select ENSP00000240093.3:n.1404+5326del
ENST00000240093.7:c.1404+5326del ENSP00000240093.3:n.1404+5326del
ENST00000537916.2:c.1404+5326del ENSP00000437489.1:n.1404+5326del
NM_017412.3:c.1404+5326del NP_059108.1:n.1404+5326del
NM_145866.1:c.1404+5326del NP_665873.1:n.1404+5326del
XM_011544646.1:c.1287+5326del XP_011542948.1:n.1287+5326del
XM_011544647.1:c.1203+5326del XP_011542949.1:n.1203+5326del
XM_011544649.1:c.1203+5326del XP_011542951.1:n.1203+5326del
XR_949476.1:n.1924-3403del
XR_949477.1:n.1924-3403del
XR_949478.1:n.1923+5326del
XM_017013841.1:c.1203+5326del XP_016869330.1:n.1203+5326del
XM_017013842.1:c.1405-3403del XP_016869331.1:n.1405-3403del
XM_017013843.1:c.1405-3403del XP_016869332.1:n.1405-3403del
XM_017013844.1:c.1404+5326del XP_016869333.1:n.1404+5326del
XR_001745597.2:n.1880+5326del
XR_949476.2:n.1924-3403del
NM_017412.4:c.1404+5326del MANE Select NP_059108.1:n.1404+5326del
NM_145866.2:c.1404+5326del NP_665873.1:n.1404+5326del