Canonical Allele Identifier: CA1773344550

Gene: FZD3

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_017412.4:c.435A= MANE Select	NP_059108.1:p.Leu145=
ENST00000240093.8:c.435A= MANE Select	ENSP00000240093.3:p.Leu145=
NM_017412.3:c.435A=	NP_059108.1:p.Leu145=
NM_145866.1:c.435A=	NP_665873.1:p.Leu145=
NM_145866.2:c.435A=	NP_665873.1:p.Leu145=
ENST00000240093.7:c.435A=	ENSP00000240093.3:p.Leu145=
ENST00000537916.2:c.435A=	ENSP00000437489.1:p.Leu145=
XM_011544646.1:c.318A=	XP_011542948.1:p.Leu106=
XM_011544647.1:c.234A=	XP_011542949.1:p.Leu78=
XM_011544648.1:c.435A=	XP_011542950.1:p.Leu145=
XM_011544649.1:c.234A=	XP_011542951.1:p.Leu78=
XM_017013841.1:c.234A=	XP_016869330.1:p.Leu78=
XM_017013842.1:c.435A=	XP_016869331.1:p.Leu145=
XM_017013843.1:c.435A=	XP_016869332.1:p.Leu145=
XM_017013844.1:c.435A=	XP_016869333.1:p.Leu145=
XR_001745597.2:n.911A=
XR_949476.1:n.954A=
XR_949476.2:n.954A=
XR_949477.1:n.954A=
XR_949478.1:n.954A=