Canonical Allele Identifier: CA2793028354

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952527_86952528del , CM000673.2:g.86952527_86952528del GRCh38
NC_000011.9:g.86663569_86663570del , CM000673.1:g.86663569_86663570del GRCh37
NC_000011.8:g.86341217_86341218del NCBI36
NG_011752.1:g.7864_7865del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.286-58_286-57del (FZD4) MANE Select ENSP00000434034.1:n.286-58_286-57del
ENST00000531380.1:c.286-58_286-57del (FZD4) ENSP00000434034.1:n.286-58_286-57del
ENST00000532234.5:c.*1520_*1521del (PRSS23) ENSP00000436676.1:n.*1520_*1521del
ENST00000533902.2:c.*1242_*1243del (PRSS23) ENSP00000437268.1:n.*1242_*1243del
NM_012193.3:c.286-58_286-57del (FZD4) NP_036325.2:n.286-58_286-57del
NR_120591.1:n.2192_2193del (PRSS23)
NR_120592.1:n.1941_1942del (PRSS23)
NR_120591.2:n.1890_1891del (PRSS23)
NR_120592.2:n.1639_1640del (PRSS23)
NM_012193.4:c.286-58_286-57del (FZD4) MANE Select NP_036325.2:n.286-58_286-57del
NR_120591.3:n.1890_1891del (PRSS23)