Canonical Allele Identifier: CA2793028371

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952536_86952537del , CM000673.2:g.86952536_86952537del GRCh38
NC_000011.9:g.86663578_86663579del , CM000673.1:g.86663578_86663579del GRCh37
NC_000011.8:g.86341226_86341227del NCBI36
NG_011752.1:g.7856_7857del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.286-66_286-65del (FZD4) MANE Select ENSP00000434034.1:n.286-66_286-65del
ENST00000531380.1:c.286-66_286-65del (FZD4) ENSP00000434034.1:n.286-66_286-65del
ENST00000532234.5:c.*1529_*1530del (PRSS23) ENSP00000436676.1:n.*1529_*1530del
ENST00000533902.2:c.*1251_*1252del (PRSS23) ENSP00000437268.1:n.*1251_*1252del
NM_012193.3:c.286-66_286-65del (FZD4) NP_036325.2:n.286-66_286-65del
NR_120591.1:n.2201_2202del (PRSS23)
NR_120592.1:n.1950_1951del (PRSS23)
NR_120591.2:n.1899_1900del (PRSS23)
NR_120592.2:n.1648_1649del (PRSS23)
NM_012193.4:c.286-66_286-65del (FZD4) MANE Select NP_036325.2:n.286-66_286-65del
NR_120591.3:n.1899_1900del (PRSS23)