Canonical Allele Identifier: CA370945266
Gene: FZD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.28527195A>C , CM000670.2:g.28527195A>C GRCh38
NC_000008.10:g.28384712A>C , CM000670.1:g.28384712A>C GRCh37
NC_000008.9:g.28440631A>C NCBI36
NG_029723.1:g.37991A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000240093.8:c.435A>C MANE Select ENSP00000240093.3:p.Leu145Phe
ENST00000240093.7:c.435A>C ENSP00000240093.3:p.Leu145Phe
ENST00000537916.2:c.435A>C ENSP00000437489.1:p.Leu145Phe
NM_017412.3:c.435A>C NP_059108.1:p.Leu145Phe
NM_145866.1:c.435A>C NP_665873.1:p.Leu145Phe
XM_011544646.1:c.318A>C XP_011542948.1:p.Leu106Phe
XM_011544647.1:c.234A>C XP_011542949.1:p.Leu78Phe
XM_011544648.1:c.435A>C XP_011542950.1:p.Leu145Phe
XM_011544649.1:c.234A>C XP_011542951.1:p.Leu78Phe
XR_949476.1:n.954A>C
XR_949477.1:n.954A>C
XR_949478.1:n.954A>C
XM_017013841.1:c.234A>C XP_016869330.1:p.Leu78Phe
XM_017013842.1:c.435A>C XP_016869331.1:p.Leu145Phe
XM_017013843.1:c.435A>C XP_016869332.1:p.Leu145Phe
XM_017013844.1:c.435A>C XP_016869333.1:p.Leu145Phe
XR_001745597.2:n.911A>C
XR_949476.2:n.954A>C
NM_017412.4:c.435A>C MANE Select NP_059108.1:p.Leu145Phe
NM_145866.2:c.435A>C NP_665873.1:p.Leu145Phe