Canonical Allele Identifier: CA1988809167

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952283C= , CM000673.2:g.86952283C= GRCh38
NC_000011.9:g.86663325C= , CM000673.1:g.86663325C= GRCh37
NC_000011.8:g.86340973C= NCBI36
NG_011752.1:g.8109G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.473G= (FZD4) MANE Select ENSP00000434034.1:p.Cys158=
ENST00000531380.1:c.473G= (FZD4) ENSP00000434034.1:p.Cys158=
ENST00000532234.5:c.*1276C= (PRSS23) ENSP00000436676.1:n.*1276C=
ENST00000533902.2:c.*998C= (PRSS23) ENSP00000437268.1:n.*998C=
NM_012193.3:c.473G= (FZD4) NP_036325.2:p.Cys158=
NR_120591.1:n.1948C= (PRSS23)
NR_120592.1:n.1697C= (PRSS23)
NR_120591.2:n.1646C= (PRSS23)
NR_120592.2:n.1395C= (PRSS23)
NM_012193.4:c.473G= (FZD4) MANE Select NP_036325.2:p.Cys158=
NR_120591.3:n.1646C= (PRSS23)