Canonical Allele Identifier: CA1773353068
Gene: FZD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28533896_28533898delinsTTG , CM000670.2:g.28533896_28533898delinsTTG GRCh38
NC_000008.10:g.28391413_28391415delinsTTG , CM000670.1:g.28391413_28391415delinsTTG GRCh37
NC_000008.9:g.28447332_28447334delinsTTG NCBI36
NG_029723.1:g.44692_44694delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000240093.8:c.1404+5732_1404+5734delinsTTG MANE Select ENSP00000240093.3:n.1404+5732_1404+5734delinsTTG
ENST00000240093.7:c.1404+5732_1404+5734delinsTTG ENSP00000240093.3:n.1404+5732_1404+5734delinsTTG
ENST00000537916.2:c.1404+5732_1404+5734delinsTTG ENSP00000437489.1:n.1404+5732_1404+5734delinsTTG
NM_017412.3:c.1404+5732_1404+5734delinsTTG NP_059108.1:n.1404+5732_1404+5734delinsTTG
NM_145866.1:c.1404+5732_1404+5734delinsTTG NP_665873.1:n.1404+5732_1404+5734delinsTTG
XM_011544646.1:c.1287+5732_1287+5734delinsTTG XP_011542948.1:n.1287+5732_1287+5734delinsTTG
XM_011544647.1:c.1203+5732_1203+5734delinsTTG XP_011542949.1:n.1203+5732_1203+5734delinsTTG
XM_011544649.1:c.1203+5732_1203+5734delinsTTG XP_011542951.1:n.1203+5732_1203+5734delinsTTG
XR_949476.1:n.1924-2997_1924-2995delinsTTG
XR_949477.1:n.1924-2997_1924-2995delinsTTG
XR_949478.1:n.1923+5732_1923+5734delinsTTG
XM_017013841.1:c.1203+5732_1203+5734delinsTTG XP_016869330.1:n.1203+5732_1203+5734delinsTTG
XM_017013842.1:c.1405-2997_1405-2995delinsTTG XP_016869331.1:n.1405-2997_1405-2995delinsTTG
XM_017013843.1:c.1405-2997_1405-2995delinsTTG XP_016869332.1:n.1405-2997_1405-2995delinsTTG
XM_017013844.1:c.1404+5732_1404+5734delinsTTG XP_016869333.1:n.1404+5732_1404+5734delinsTTG
XR_001745597.2:n.1880+5732_1880+5734delinsTTG
XR_949476.2:n.1924-2997_1924-2995delinsTTG
NM_017412.4:c.1404+5732_1404+5734delinsTTG MANE Select NP_059108.1:n.1404+5732_1404+5734delinsTTG
NM_145866.2:c.1404+5732_1404+5734delinsTTG NP_665873.1:n.1404+5732_1404+5734delinsTTG