Canonical Allele Identifier: CA1988807159

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950875C= , CM000673.2:g.86950875C= GRCh38
NC_000011.9:g.86661917C= , CM000673.1:g.86661917C= GRCh37
NC_000011.8:g.86339565C= NCBI36
NG_011752.1:g.9517G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*267G= (FZD4) MANE Select ENSP00000434034.1:n.*267G=
ENST00000528769.5:n.273-341C= (PRSS23)
ENST00000531380.1:c.*267G= (FZD4) ENSP00000434034.1:n.*267G=
ENST00000531521.1:n.387-341C= (PRSS23)
ENST00000532234.5:c.*209-341C= (PRSS23) ENSP00000436676.1:n.*209-341C=
ENST00000533902.2:c.207-341C= (PRSS23) ENSP00000437268.1:n.207-341C=
NM_012193.3:c.*267G= (FZD4) NP_036325.2:n.*267G=
NR_120591.1:n.881-341C= (PRSS23)
NR_120592.1:n.630-341C= (PRSS23)
NR_120591.2:n.579-341C= (PRSS23)
NR_120592.2:n.328-341C= (PRSS23)
NM_012193.4:c.*267G= (FZD4) MANE Select NP_036325.2:n.*267G=
NR_120591.3:n.579-341C= (PRSS23)