Canonical Allele Identifier: CA2695215105

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951428_86951432del , CM000673.2:g.86951428_86951432del GRCh38
NC_000011.9:g.86662470_86662474del , CM000673.1:g.86662470_86662474del GRCh37
NC_000011.8:g.86340118_86340122del NCBI36
NG_011752.1:g.8964_8968del

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1328_1332del (FZD4) MANE Select ENSP00000434034.1:p.Leu443HisfsTer14
ENST00000531380.1:c.1328_1332del (FZD4) ENSP00000434034.1:p.Leu443HisfsTer14
ENST00000531521.1:n.599_603del (PRSS23)
ENST00000532234.5:c.*421_*425del (PRSS23) ENSP00000436676.1:n.*421_*425del
ENST00000533902.2:c.*143_*147del (PRSS23) ENSP00000437268.1:n.*143_*147del
NM_012193.3:c.1328_1332del (FZD4) NP_036325.2:p.Leu443HisfsTer14
NR_120591.1:n.1093_1097del (PRSS23)
NR_120592.1:n.842_846del (PRSS23)
NR_120591.2:n.791_795del (PRSS23)
NR_120592.2:n.540_544del (PRSS23)
NM_012193.4:c.1328_1332del (FZD4) MANE Select NP_036325.2:p.Leu443HisfsTer14
NR_120591.3:n.791_795del (PRSS23)