Canonical Allele Identifier: CA225380385

Linked Data

dbSNP Id: rs80358302

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951261del , CM000673.2:g.86951261del GRCh38
NC_000011.9:g.86662303del , CM000673.1:g.86662303del GRCh37
NC_000011.8:g.86339951del NCBI36
NG_011752.1:g.9134del

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1498del (FZD4) MANE Select ENSP00000434034.1:p.Thr500LeufsTer13
ENST00000528769.5:n.318del (PRSS23)
ENST00000531380.1:c.1498del (FZD4) ENSP00000434034.1:p.Thr500LeufsTer13
ENST00000531521.1:n.432del (PRSS23)
ENST00000532234.5:c.*254del (PRSS23) ENSP00000436676.1:n.*254del
ENST00000533902.2:c.252del (PRSS23) ENSP00000437268.1:p.Phe84LeufsTer?
NM_012193.3:c.1498del (FZD4) NP_036325.2:p.Thr500LeufsTer13
NR_120591.1:n.926del (PRSS23)
NR_120592.1:n.675del (PRSS23)
NR_120591.2:n.624del (PRSS23)
NR_120592.2:n.373del (PRSS23)
NM_012193.4:c.1498del (FZD4) MANE Select NP_036325.2:p.Thr500LeufsTer13
NR_120591.3:n.624del (PRSS23)