Canonical Allele Identifier: CA1988807358

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951071_86951074delinsTTAG , CM000673.2:g.86951071_86951074delinsTTAG GRCh38
NC_000011.9:g.86662113_86662116delinsTTAG , CM000673.1:g.86662113_86662116delinsTTAG GRCh37
NC_000011.8:g.86339761_86339764delinsTTAG NCBI36
NG_011752.1:g.9318_9321delinsCTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*68_*71delinsCTAA (FZD4) MANE Select ENSP00000434034.1:n.*68_*71delinsCTAA
ENST00000528769.5:n.273-145_273-142delinsTTAG (PRSS23)
ENST00000531380.1:c.*68_*71delinsCTAA (FZD4) ENSP00000434034.1:n.*68_*71delinsCTAA
ENST00000531521.1:n.387-145_387-142delinsTTAG (PRSS23)
ENST00000532234.5:c.*209-145_*209-142delinsTTAG (PRSS23) ENSP00000436676.1:n.*209-145_*209-142delinsTTAG
ENST00000533902.2:c.207-145_207-142delinsTTAG (PRSS23) ENSP00000437268.1:n.207-145_207-142delinsTTAG
NM_012193.3:c.*68_*71delinsCTAA (FZD4) NP_036325.2:n.*68_*71delinsCTAA
NR_120591.1:n.881-145_881-142delinsTTAG (PRSS23)
NR_120592.1:n.630-145_630-142delinsTTAG (PRSS23)
NR_120591.2:n.579-145_579-142delinsTTAG (PRSS23)
NR_120592.2:n.328-145_328-142delinsTTAG (PRSS23)
NM_012193.4:c.*68_*71delinsCTAA (FZD4) MANE Select NP_036325.2:n.*68_*71delinsCTAA
NR_120591.3:n.579-145_579-142delinsTTAG (PRSS23)