Canonical Allele Identifier: CA2615460877

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950816del , CM000673.2:g.86950816del GRCh38
NC_000011.9:g.86661858del , CM000673.1:g.86661858del GRCh37
NC_000011.8:g.86339506del NCBI36
NG_011752.1:g.9579del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*329del (FZD4) MANE Select ENSP00000434034.1:n.*329del
ENST00000528769.5:n.272+317del (PRSS23)
ENST00000531380.1:c.*329del (FZD4) ENSP00000434034.1:n.*329del
ENST00000531521.1:n.386+317del (PRSS23)
ENST00000532234.5:c.*208+317del (PRSS23) ENSP00000436676.1:n.*208+317del
ENST00000533902.2:c.207-400del (PRSS23) ENSP00000437268.1:n.207-400del
NM_012193.3:c.*329del (FZD4) NP_036325.2:n.*329del
NR_120591.1:n.880+317del (PRSS23)
NR_120592.1:n.630-400del (PRSS23)
NR_120591.2:n.578+317del (PRSS23)
NR_120592.2:n.328-400del (PRSS23)
NM_012193.4:c.*329del (FZD4) MANE Select NP_036325.2:n.*329del
NR_120591.3:n.578+317del (PRSS23)