Canonical Allele Identifier: CA2615461142

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950980_86950989del , CM000673.2:g.86950980_86950989del GRCh38
NC_000011.9:g.86662022_86662031del , CM000673.1:g.86662022_86662031del GRCh37
NC_000011.8:g.86339670_86339679del NCBI36
NG_011752.1:g.9403_9412del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*153_*162del (FZD4) MANE Select ENSP00000434034.1:n.*153_*162del
ENST00000528769.5:n.273-236_273-227del (PRSS23)
ENST00000531380.1:c.*153_*162del (FZD4) ENSP00000434034.1:n.*153_*162del
ENST00000531521.1:n.387-236_387-227del (PRSS23)
ENST00000532234.5:c.*209-236_*209-227del (PRSS23) ENSP00000436676.1:n.*209-236_*209-227del
ENST00000533902.2:c.207-236_207-227del (PRSS23) ENSP00000437268.1:n.207-236_207-227del
NM_012193.3:c.*153_*162del (FZD4) NP_036325.2:n.*153_*162del
NR_120591.1:n.881-236_881-227del (PRSS23)
NR_120592.1:n.630-236_630-227del (PRSS23)
NR_120591.2:n.579-236_579-227del (PRSS23)
NR_120592.2:n.328-236_328-227del (PRSS23)
NM_012193.4:c.*153_*162del (FZD4) MANE Select NP_036325.2:n.*153_*162del
NR_120591.3:n.579-236_579-227del (PRSS23)