Canonical Allele Identifier: CA1988808839

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952073C= , CM000673.2:g.86952073C= GRCh38
NC_000011.9:g.86663115C= , CM000673.1:g.86663115C= GRCh37
NC_000011.8:g.86340763C= NCBI36
NG_011752.1:g.8319G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.683G= (FZD4) MANE Select ENSP00000434034.1:p.Ser228=
ENST00000531380.1:c.683G= (FZD4) ENSP00000434034.1:p.Ser228=
ENST00000532234.5:c.*1066C= (PRSS23) ENSP00000436676.1:n.*1066C=
ENST00000533902.2:c.*788C= (PRSS23) ENSP00000437268.1:n.*788C=
NM_012193.3:c.683G= (FZD4) NP_036325.2:p.Ser228=
NR_120591.1:n.1738C= (PRSS23)
NR_120592.1:n.1487C= (PRSS23)
NR_120591.2:n.1436C= (PRSS23)
NR_120592.2:n.1185C= (PRSS23)
NM_012193.4:c.683G= (FZD4) MANE Select NP_036325.2:p.Ser228=
NR_120591.3:n.1436C= (PRSS23)