Canonical Allele Identifier: CA1988802582

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86946496C= , CM000673.2:g.86946496C= GRCh38
NC_000011.9:g.86657538C= , CM000673.1:g.86657538C= GRCh37
NC_000011.8:g.86335186C= NCBI36
NG_011752.1:g.13896G=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.*4646G= (FZD4) MANE Select ENSP00000434034.1:n.*4646G=
ENST00000528769.5:n.129-3860C= (PRSS23)
ENST00000531380.1:c.*4646G= (FZD4) ENSP00000434034.1:n.*4646G=
ENST00000531521.1:n.243-3860C= (PRSS23)
ENST00000532234.5:c.*65-3860C= (PRSS23) ENSP00000436676.1:n.*65-3860C=
ENST00000533902.2:c.207-4720C= (PRSS23) ENSP00000437268.1:n.207-4720C=
NM_012193.3:c.*4646G= (FZD4) NP_036325.2:n.*4646G=
NR_120591.1:n.737-3860C= (PRSS23)
NR_120592.1:n.630-4720C= (PRSS23)
NR_120591.2:n.435-3860C= (PRSS23)
NR_120592.2:n.328-4720C= (PRSS23)
NM_012193.4:c.*4646G= (FZD4) MANE Select NP_036325.2:n.*4646G=
NR_120591.3:n.435-3860C= (PRSS23)