Canonical Allele Identifier: CA1988807038

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950744A= , CM000673.2:g.86950744A= GRCh38
NC_000011.9:g.86661786A= , CM000673.1:g.86661786A= GRCh37
NC_000011.8:g.86339434A= NCBI36
NG_011752.1:g.9648T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*398T= (FZD4) MANE Select ENSP00000434034.1:n.*398T=
ENST00000528769.5:n.272+245A= (PRSS23)
ENST00000531380.1:c.*398T= (FZD4) ENSP00000434034.1:n.*398T=
ENST00000531521.1:n.386+245A= (PRSS23)
ENST00000532234.5:c.*208+245A= (PRSS23) ENSP00000436676.1:n.*208+245A=
ENST00000533902.2:c.207-472A= (PRSS23) ENSP00000437268.1:n.207-472A=
NM_012193.3:c.*398T= (FZD4) NP_036325.2:n.*398T=
NR_120591.1:n.880+245A= (PRSS23)
NR_120592.1:n.630-472A= (PRSS23)
NR_120591.2:n.578+245A= (PRSS23)
NR_120592.2:n.328-472A= (PRSS23)
NM_012193.4:c.*398T= (FZD4) MANE Select NP_036325.2:n.*398T=
NR_120591.3:n.578+245A= (PRSS23)