Canonical Allele Identifier: CA1988807058

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950777T= , CM000673.2:g.86950777T= GRCh38
NC_000011.9:g.86661819T= , CM000673.1:g.86661819T= GRCh37
NC_000011.8:g.86339467T= NCBI36
NG_011752.1:g.9615A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*365A= (FZD4) MANE Select ENSP00000434034.1:n.*365A=
ENST00000528769.5:n.272+278T= (PRSS23)
ENST00000531380.1:c.*365A= (FZD4) ENSP00000434034.1:n.*365A=
ENST00000531521.1:n.386+278T= (PRSS23)
ENST00000532234.5:c.*208+278T= (PRSS23) ENSP00000436676.1:n.*208+278T=
ENST00000533902.2:c.207-439T= (PRSS23) ENSP00000437268.1:n.207-439T=
NM_012193.3:c.*365A= (FZD4) NP_036325.2:n.*365A=
NR_120591.1:n.880+278T= (PRSS23)
NR_120592.1:n.630-439T= (PRSS23)
NR_120591.2:n.578+278T= (PRSS23)
NR_120592.2:n.328-439T= (PRSS23)
NM_012193.4:c.*365A= (FZD4) MANE Select NP_036325.2:n.*365A=
NR_120591.3:n.578+278T= (PRSS23)