Canonical Allele Identifier: CA1773352904

Gene: FZD3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28533577_28533597delinsGTTTGTTTTGTTTTGTTTTGT , CM000670.2:g.28533577_28533597delinsGTTTGTTTTGTTTTGTTTTGT	GRCh38
NC_000008.10:g.28391094_28391114delinsGTTTGTTTTGTTTTGTTTTGT , CM000670.1:g.28391094_28391114delinsGTTTGTTTTGTTTTGTTTTGT	GRCh37
NC_000008.9:g.28447013_28447033delinsGTTTGTTTTGTTTTGTTTTGT	NCBI36
NG_029723.1:g.44373_44393delinsGTTTGTTTTGTTTTGTTTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000240093.8:c.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT MANE Select	ENSP00000240093.3:n.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGT...
ENST00000240093.7:c.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT	ENSP00000240093.3:n.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGT...
ENST00000537916.2:c.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT	ENSP00000437489.1:n.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGT...
NM_017412.3:c.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT	NP_059108.1:n.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT
NM_145866.1:c.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT	NP_665873.1:n.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT
XM_011544646.1:c.1287+5413_1287+5433delinsGTTTGTTTTGTTTTGTTTTGT	XP_011542948.1:n.1287+5413_1287+5433delinsGTTTGTTTTGTTTTGTTTT...
XM_011544647.1:c.1203+5413_1203+5433delinsGTTTGTTTTGTTTTGTTTTGT	XP_011542949.1:n.1203+5413_1203+5433delinsGTTTGTTTTGTTTTGTTTT...
XM_011544649.1:c.1203+5413_1203+5433delinsGTTTGTTTTGTTTTGTTTTGT	XP_011542951.1:n.1203+5413_1203+5433delinsGTTTGTTTTGTTTTGTTTT...
XR_949476.1:n.1924-3316_1924-3296delinsGTTTGTTTTGTTTTGTTTTGT
XR_949477.1:n.1924-3316_1924-3296delinsGTTTGTTTTGTTTTGTTTTGT
XR_949478.1:n.1923+5413_1923+5433delinsGTTTGTTTTGTTTTGTTTTGT
XM_017013841.1:c.1203+5413_1203+5433delinsGTTTGTTTTGTTTTGTTTTGT	XP_016869330.1:n.1203+5413_1203+5433delinsGTTTGTTTTGTTTTGTTTT...
XM_017013842.1:c.1405-3316_1405-3296delinsGTTTGTTTTGTTTTGTTTTGT	XP_016869331.1:n.1405-3316_1405-3296delinsGTTTGTTTTGTTTTGTTTT...
XM_017013843.1:c.1405-3316_1405-3296delinsGTTTGTTTTGTTTTGTTTTGT	XP_016869332.1:n.1405-3316_1405-3296delinsGTTTGTTTTGTTTTGTTTT...
XM_017013844.1:c.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT	XP_016869333.1:n.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTT...
XR_001745597.2:n.1880+5413_1880+5433delinsGTTTGTTTTGTTTTGTTTTGT
XR_949476.2:n.1924-3316_1924-3296delinsGTTTGTTTTGTTTTGTTTTGT
NM_017412.4:c.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT MANE Select	NP_059108.1:n.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT
NM_145866.2:c.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT	NP_665873.1:n.1404+5413_1404+5433delinsGTTTGTTTTGTTTTGTTTTGT