Canonical Allele Identifier: CA1112202695
Gene: FZD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28533620_28533628del , CM000670.2:g.28533620_28533628del GRCh38
NC_000008.10:g.28391137_28391145del , CM000670.1:g.28391137_28391145del GRCh37
NC_000008.9:g.28447056_28447064del NCBI36
NG_029723.1:g.44416_44424del

Transcript Alleles

HGVS Amino-acid Change
ENST00000240093.8:c.1404+5456_1404+5464del MANE Select ENSP00000240093.3:n.1404+5456_1404+5464del
ENST00000240093.7:c.1404+5456_1404+5464del ENSP00000240093.3:n.1404+5456_1404+5464del
ENST00000537916.2:c.1404+5456_1404+5464del ENSP00000437489.1:n.1404+5456_1404+5464del
NM_017412.3:c.1404+5456_1404+5464del NP_059108.1:n.1404+5456_1404+5464del
NM_145866.1:c.1404+5456_1404+5464del NP_665873.1:n.1404+5456_1404+5464del
XM_011544646.1:c.1287+5456_1287+5464del XP_011542948.1:n.1287+5456_1287+5464del
XM_011544647.1:c.1203+5456_1203+5464del XP_011542949.1:n.1203+5456_1203+5464del
XM_011544649.1:c.1203+5456_1203+5464del XP_011542951.1:n.1203+5456_1203+5464del
XR_949476.1:n.1924-3273_1924-3265del
XR_949477.1:n.1924-3273_1924-3265del
XR_949478.1:n.1923+5456_1923+5464del
XM_017013841.1:c.1203+5456_1203+5464del XP_016869330.1:n.1203+5456_1203+5464del
XM_017013842.1:c.1405-3273_1405-3265del XP_016869331.1:n.1405-3273_1405-3265del
XM_017013843.1:c.1405-3273_1405-3265del XP_016869332.1:n.1405-3273_1405-3265del
XM_017013844.1:c.1404+5456_1404+5464del XP_016869333.1:n.1404+5456_1404+5464del
XR_001745597.2:n.1880+5456_1880+5464del
XR_949476.2:n.1924-3273_1924-3265del
NM_017412.4:c.1404+5456_1404+5464del MANE Select NP_059108.1:n.1404+5456_1404+5464del
NM_145866.2:c.1404+5456_1404+5464del NP_665873.1:n.1404+5456_1404+5464del