Canonical Allele Identifier: CA681338108

Linked Data

dbSNP Id: rs1367877171

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951018_86951019del , CM000673.2:g.86951018_86951019del GRCh38
NC_000011.9:g.86662060_86662061del , CM000673.1:g.86662060_86662061del GRCh37
NC_000011.8:g.86339708_86339709del NCBI36
NG_011752.1:g.9376_9377del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*126_*127del (FZD4) MANE Select ENSP00000434034.1:n.*126_*127del
ENST00000528769.5:n.273-198_273-197del (PRSS23)
ENST00000531380.1:c.*126_*127del (FZD4) ENSP00000434034.1:n.*126_*127del
ENST00000531521.1:n.387-198_387-197del (PRSS23)
ENST00000532234.5:c.*209-198_*209-197del (PRSS23) ENSP00000436676.1:n.*209-198_*209-197del
ENST00000533902.2:c.207-198_207-197del (PRSS23) ENSP00000437268.1:n.207-198_207-197del
NM_012193.3:c.*126_*127del (FZD4) NP_036325.2:n.*126_*127del
NR_120591.1:n.881-198_881-197del (PRSS23)
NR_120592.1:n.630-198_630-197del (PRSS23)
NR_120591.2:n.579-198_579-197del (PRSS23)
NR_120592.2:n.328-198_328-197del (PRSS23)
NM_012193.4:c.*126_*127del (FZD4) MANE Select NP_036325.2:n.*126_*127del
NR_120591.3:n.579-198_579-197del (PRSS23)