Canonical Allele Identifier: CA1807177254
Gene: FZD6 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000358755.5:c.1531C= MANE Select ENSP00000351605.4:p.Arg511=
ENST00000358755.4:c.1531C= ENSP00000351605.4:p.Arg511=
ENST00000519011.5:c.*578C= ENSP00000427733.1:n.*578C=
ENST00000521195.1:c.*1466C= ENSP00000428188.1:n.*1466C=
ENST00000522484.5:c.1393-1249C= ENSP00000428301.1:n.1393-1249C=
ENST00000522566.5:c.1531C= ENSP00000429055.1:p.Arg511=
ENST00000523739.5:c.1435C= ENSP00000429528.1:p.Arg479=
ENST00000523933.5:c.*578C= ENSP00000428257.1:n.*578C=
NM_001164615.1:c.1531C= NP_001158087.1:p.Arg511=
NM_001164616.1:c.1435C= NP_001158088.1:p.Arg479=
NM_003506.3:c.1531C= NP_003497.2:p.Arg511=
XR_428385.2:n.1643-1249C=
NM_001317796.1:c.616C= NP_001304725.1:p.Arg206=
NR_133921.1:n.1710-1249C=
NM_003506.4:c.1531C= MANE Select NP_003497.2:p.Arg511=
NM_001164615.2:c.1531C= NP_001158087.1:p.Arg511=
NM_001164616.2:c.1435C= NP_001158088.1:p.Arg479=
NM_001317796.2:c.616C= NP_001304725.1:p.Arg206=
NR_133921.2:n.1710-1249C=