Canonical Allele Identifier: CA129147
Gene: FZD6 HGNC NCBI

Linked Data

ClinVar Variation Id: 30356
dbSNP Id: rs151339003

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.103328406C>T , CM000670.2:g.103328406C>T GRCh38
NC_000008.10:g.104340634C>T , CM000670.1:g.104340634C>T GRCh37
NC_000008.9:g.104409810C>T NCBI36
NG_028909.1:g.34974C>T
NG_028909.2:g.32413C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000358755.5:c.1531C>T MANE Select ENSP00000351605.4:p.Arg511Cys
ENST00000358755.4:c.1531C>T ENSP00000351605.4:p.Arg511Cys
ENST00000519011.5:c.*578C>T ENSP00000427733.1:n.*578C>T
ENST00000521195.1:c.*1466C>T ENSP00000428188.1:n.*1466C>T
ENST00000522484.5:c.1393-1249C>T ENSP00000428301.1:n.1393-1249C>T
ENST00000522566.5:c.1531C>T ENSP00000429055.1:p.Arg511Cys
ENST00000523739.5:c.1435C>T ENSP00000429528.1:p.Arg479Cys
ENST00000523933.5:c.*578C>T ENSP00000428257.1:n.*578C>T
NM_001164615.1:c.1531C>T NP_001158087.1:p.Arg511Cys
NM_001164616.1:c.1435C>T NP_001158088.1:p.Arg479Cys
NM_003506.3:c.1531C>T NP_003497.2:p.Arg511Cys
XR_428385.2:n.1643-1249C>T
NM_001317796.1:c.616C>T NP_001304725.1:p.Arg206Cys
NR_133921.1:n.1710-1249C>T
NM_003506.4:c.1531C>T MANE Select NP_003497.2:p.Arg511Cys
NM_001164615.2:c.1531C>T NP_001158087.1:p.Arg511Cys
NM_001164616.2:c.1435C>T NP_001158088.1:p.Arg479Cys
NM_001317796.2:c.616C>T NP_001304725.1:p.Arg206Cys
NR_133921.2:n.1710-1249C>T