Canonical Allele Identifier: CA1988809233

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952339C= , CM000673.2:g.86952339C= GRCh38
NC_000011.9:g.86663381C= , CM000673.1:g.86663381C= GRCh37
NC_000011.8:g.86341029C= NCBI36
NG_011752.1:g.8053G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.417G= (FZD4) MANE Select ENSP00000434034.1:p.Trp139=
ENST00000531380.1:c.417G= (FZD4) ENSP00000434034.1:p.Trp139=
ENST00000532234.5:c.*1332C= (PRSS23) ENSP00000436676.1:n.*1332C=
ENST00000533902.2:c.*1054C= (PRSS23) ENSP00000437268.1:n.*1054C=
NM_012193.3:c.417G= (FZD4) NP_036325.2:p.Trp139=
NR_120591.1:n.2004C= (PRSS23)
NR_120592.1:n.1753C= (PRSS23)
NR_120591.2:n.1702C= (PRSS23)
NR_120592.2:n.1451C= (PRSS23)
NM_012193.4:c.417G= (FZD4) MANE Select NP_036325.2:p.Trp139=
NR_120591.3:n.1702C= (PRSS23)