Canonical Allele Identifier: CA850493482

Gene: FZD3

Linked Data

• dbSNP Id: rs1230961707
• gnomAD v3: 8-28533402-CT-C
• gnomAD v4: 8-28533402-CT-C
• MyVariant Identifiers: chr8:g.28390920del (hg19) ; chr8:g.28533403del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.28533405del , CM000670.2:g.28533405del	GRCh38
NC_000008.10:g.28390922del , CM000670.1:g.28390922del	GRCh37
NC_000008.9:g.28446841del	NCBI36
NG_029723.1:g.44201del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000240093.8:c.1404+5241del MANE Select	ENSP00000240093.3:n.1404+5241del
ENST00000240093.7:c.1404+5241del	ENSP00000240093.3:n.1404+5241del
ENST00000537916.2:c.1404+5241del	ENSP00000437489.1:n.1404+5241del
NM_017412.3:c.1404+5241del	NP_059108.1:n.1404+5241del
NM_145866.1:c.1404+5241del	NP_665873.1:n.1404+5241del
XM_011544646.1:c.1287+5241del	XP_011542948.1:n.1287+5241del
XM_011544647.1:c.1203+5241del	XP_011542949.1:n.1203+5241del
XM_011544649.1:c.1203+5241del	XP_011542951.1:n.1203+5241del
XR_949476.1:n.1924-3488del
XR_949477.1:n.1924-3488del
XR_949478.1:n.1923+5241del
XM_017013841.1:c.1203+5241del	XP_016869330.1:n.1203+5241del
XM_017013842.1:c.1405-3488del	XP_016869331.1:n.1405-3488del
XM_017013843.1:c.1405-3488del	XP_016869332.1:n.1405-3488del
XM_017013844.1:c.1404+5241del	XP_016869333.1:n.1404+5241del
XR_001745597.2:n.1880+5241del
XR_949476.2:n.1924-3488del
NM_017412.4:c.1404+5241del MANE Select	NP_059108.1:n.1404+5241del
NM_145866.2:c.1404+5241del	NP_665873.1:n.1404+5241del