Canonical Allele Identifier: CA1773353055

Gene: FZD3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28533882T= , CM000670.2:g.28533882T=	GRCh38
NC_000008.10:g.28391399T= , CM000670.1:g.28391399T=	GRCh37
NC_000008.9:g.28447318T=	NCBI36
NG_029723.1:g.44678T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000240093.8:c.1404+5718T= MANE Select	ENSP00000240093.3:n.1404+5718T=
ENST00000240093.7:c.1404+5718T=	ENSP00000240093.3:n.1404+5718T=
ENST00000537916.2:c.1404+5718T=	ENSP00000437489.1:n.1404+5718T=
NM_017412.3:c.1404+5718T=	NP_059108.1:n.1404+5718T=
NM_145866.1:c.1404+5718T=	NP_665873.1:n.1404+5718T=
XM_011544646.1:c.1287+5718T=	XP_011542948.1:n.1287+5718T=
XM_011544647.1:c.1203+5718T=	XP_011542949.1:n.1203+5718T=
XM_011544649.1:c.1203+5718T=	XP_011542951.1:n.1203+5718T=
XR_949476.1:n.1924-3011T=
XR_949477.1:n.1924-3011T=
XR_949478.1:n.1923+5718T=
XM_017013841.1:c.1203+5718T=	XP_016869330.1:n.1203+5718T=
XM_017013842.1:c.1405-3011T=	XP_016869331.1:n.1405-3011T=
XM_017013843.1:c.1405-3011T=	XP_016869332.1:n.1405-3011T=
XM_017013844.1:c.1404+5718T=	XP_016869333.1:n.1404+5718T=
XR_001745597.2:n.1880+5718T=
XR_949476.2:n.1924-3011T=
NM_017412.4:c.1404+5718T= MANE Select	NP_059108.1:n.1404+5718T=
NM_145866.2:c.1404+5718T=	NP_665873.1:n.1404+5718T=