Canonical Allele Identifier: CA1773352902
Gene: FZD3 HGNC NCBI

Linked Data

dbSNP Id: rs1804932971

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28533576_28533577insATTT , CM000670.2:g.28533576_28533577insATTT GRCh38
NC_000008.10:g.28391093_28391094insATTT , CM000670.1:g.28391093_28391094insATTT GRCh37
NC_000008.9:g.28447012_28447013insATTT NCBI36
NG_029723.1:g.44372_44373insATTT

Transcript Alleles

HGVS Amino-acid change
ENST00000240093.8:c.1404+5412_1404+5413insATTT MANE Select ENSP00000240093.3:n.1404+5412_1404+5413insATTT
ENST00000240093.7:c.1404+5412_1404+5413insATTT ENSP00000240093.3:n.1404+5412_1404+5413insATTT
ENST00000537916.2:c.1404+5412_1404+5413insATTT ENSP00000437489.1:n.1404+5412_1404+5413insATTT
NM_017412.3:c.1404+5412_1404+5413insATTT NP_059108.1:n.1404+5412_1404+5413insATTT
NM_145866.1:c.1404+5412_1404+5413insATTT NP_665873.1:n.1404+5412_1404+5413insATTT
XM_011544646.1:c.1287+5412_1287+5413insATTT XP_011542948.1:n.1287+5412_1287+5413insATTT
XM_011544647.1:c.1203+5412_1203+5413insATTT XP_011542949.1:n.1203+5412_1203+5413insATTT
XM_011544649.1:c.1203+5412_1203+5413insATTT XP_011542951.1:n.1203+5412_1203+5413insATTT
XR_949476.1:n.1924-3317_1924-3316insATTT
XR_949477.1:n.1924-3317_1924-3316insATTT
XR_949478.1:n.1923+5412_1923+5413insATTT
XM_017013841.1:c.1203+5412_1203+5413insATTT XP_016869330.1:n.1203+5412_1203+5413insATTT
XM_017013842.1:c.1405-3317_1405-3316insATTT XP_016869331.1:n.1405-3317_1405-3316insATTT
XM_017013843.1:c.1405-3317_1405-3316insATTT XP_016869332.1:n.1405-3317_1405-3316insATTT
XM_017013844.1:c.1404+5412_1404+5413insATTT XP_016869333.1:n.1404+5412_1404+5413insATTT
XR_001745597.2:n.1880+5412_1880+5413insATTT
XR_949476.2:n.1924-3317_1924-3316insATTT
NM_017412.4:c.1404+5412_1404+5413insATTT MANE Select NP_059108.1:n.1404+5412_1404+5413insATTT
NM_145866.2:c.1404+5412_1404+5413insATTT NP_665873.1:n.1404+5412_1404+5413insATTT