Canonical Allele Identifier: CA2793028843

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950745_86950746insACA , CM000673.2:g.86950745_86950746insACA GRCh38
NC_000011.9:g.86661787_86661788insACA , CM000673.1:g.86661787_86661788insACA GRCh37
NC_000011.8:g.86339435_86339436insACA NCBI36
NG_011752.1:g.9646_9647insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*396_*397insTGT (FZD4) MANE Select ENSP00000434034.1:n.*396_*397insTGT
ENST00000528769.5:n.272+246_272+247insACA (PRSS23)
ENST00000531380.1:c.*396_*397insTGT (FZD4) ENSP00000434034.1:n.*396_*397insTGT
ENST00000531521.1:n.386+246_386+247insACA (PRSS23)
ENST00000532234.5:c.*208+246_*208+247insACA (PRSS23) ENSP00000436676.1:n.*208+246_*208+247insACA
ENST00000533902.2:c.207-471_207-470insACA (PRSS23) ENSP00000437268.1:n.207-471_207-470insACA
NM_012193.3:c.*396_*397insTGT (FZD4) NP_036325.2:n.*396_*397insTGT
NR_120591.1:n.880+246_880+247insACA (PRSS23)
NR_120592.1:n.630-471_630-470insACA (PRSS23)
NR_120591.2:n.578+246_578+247insACA (PRSS23)
NR_120592.2:n.328-471_328-470insACA (PRSS23)
NM_012193.4:c.*396_*397insTGT (FZD4) MANE Select NP_036325.2:n.*396_*397insTGT
NR_120591.3:n.578+246_578+247insACA (PRSS23)