Canonical Allele Identifier: CA1988807362

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951073A= , CM000673.2:g.86951073A= GRCh38
NC_000011.9:g.86662115A= , CM000673.1:g.86662115A= GRCh37
NC_000011.8:g.86339763A= NCBI36
NG_011752.1:g.9319T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*69T= (FZD4) MANE Select ENSP00000434034.1:n.*69T=
ENST00000528769.5:n.273-143A= (PRSS23)
ENST00000531380.1:c.*69T= (FZD4) ENSP00000434034.1:n.*69T=
ENST00000531521.1:n.387-143A= (PRSS23)
ENST00000532234.5:c.*209-143A= (PRSS23) ENSP00000436676.1:n.*209-143A=
ENST00000533902.2:c.207-143A= (PRSS23) ENSP00000437268.1:n.207-143A=
NM_012193.3:c.*69T= (FZD4) NP_036325.2:n.*69T=
NR_120591.1:n.881-143A= (PRSS23)
NR_120592.1:n.630-143A= (PRSS23)
NR_120591.2:n.579-143A= (PRSS23)
NR_120592.2:n.328-143A= (PRSS23)
NM_012193.4:c.*69T= (FZD4) MANE Select NP_036325.2:n.*69T=
NR_120591.3:n.579-143A= (PRSS23)