Canonical Allele Identifier: CA2695215121

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952272del , CM000673.2:g.86952272del GRCh38
NC_000011.9:g.86663314del , CM000673.1:g.86663314del GRCh37
NC_000011.8:g.86340962del NCBI36
NG_011752.1:g.8121del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.485del (FZD4) MANE Select ENSP00000434034.1:p.Pro162GlnfsTer?
ENST00000531380.1:c.485del (FZD4) ENSP00000434034.1:p.Pro162GlnfsTer?
ENST00000532234.5:c.*1265del (PRSS23) ENSP00000436676.1:n.*1265del
ENST00000533902.2:c.*987del (PRSS23) ENSP00000437268.1:n.*987del
NM_012193.3:c.485del (FZD4) NP_036325.2:p.Pro162GlnfsTer?
NR_120591.1:n.1937del (PRSS23)
NR_120592.1:n.1686del (PRSS23)
NR_120591.2:n.1635del (PRSS23)
NR_120592.2:n.1384del (PRSS23)
NM_012193.4:c.485del (FZD4) MANE Select NP_036325.2:p.Pro162GlnfsTer?
NR_120591.3:n.1635del (PRSS23)