Canonical Allele Identifier: CA1988807676

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951247C= , CM000673.2:g.86951247C= GRCh38
NC_000011.9:g.86662289C= , CM000673.1:g.86662289C= GRCh37
NC_000011.8:g.86339937C= NCBI36
NG_011752.1:g.9145G=

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1509G= (FZD4) MANE Select ENSP00000434034.1:p.Thr503=
ENST00000528769.5:n.304C= (PRSS23)
ENST00000531380.1:c.1509G= (FZD4) ENSP00000434034.1:p.Thr503=
ENST00000531521.1:n.418C= (PRSS23)
ENST00000532234.5:c.*240C= (PRSS23) ENSP00000436676.1:n.*240C=
ENST00000533902.2:c.238C= (PRSS23) ENSP00000437268.1:p.Arg80=
NM_012193.3:c.1509G= (FZD4) NP_036325.2:p.Thr503=
NR_120591.1:n.912C= (PRSS23)
NR_120592.1:n.661C= (PRSS23)
NR_120591.2:n.610C= (PRSS23)
NR_120592.2:n.359C= (PRSS23)
NM_012193.4:c.1509G= (FZD4) MANE Select NP_036325.2:p.Thr503=
NR_120591.3:n.610C= (PRSS23)