Canonical Allele Identifier: CA1988807150

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950864C= , CM000673.2:g.86950864C= GRCh38
NC_000011.9:g.86661906C= , CM000673.1:g.86661906C= GRCh37
NC_000011.8:g.86339554C= NCBI36
NG_011752.1:g.9528G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*278G= (FZD4) MANE Select ENSP00000434034.1:n.*278G=
ENST00000528769.5:n.273-352C= (PRSS23)
ENST00000531380.1:c.*278G= (FZD4) ENSP00000434034.1:n.*278G=
ENST00000531521.1:n.387-352C= (PRSS23)
ENST00000532234.5:c.*209-352C= (PRSS23) ENSP00000436676.1:n.*209-352C=
ENST00000533902.2:c.207-352C= (PRSS23) ENSP00000437268.1:n.207-352C=
NM_012193.3:c.*278G= (FZD4) NP_036325.2:n.*278G=
NR_120591.1:n.881-352C= (PRSS23)
NR_120592.1:n.630-352C= (PRSS23)
NR_120591.2:n.579-352C= (PRSS23)
NR_120592.2:n.328-352C= (PRSS23)
NM_012193.4:c.*278G= (FZD4) MANE Select NP_036325.2:n.*278G=
NR_120591.3:n.579-352C= (PRSS23)