Canonical Allele Identifier: CA2793028278

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952457_86952459del , CM000673.2:g.86952457_86952459del GRCh38
NC_000011.9:g.86663499_86663501del , CM000673.1:g.86663499_86663501del GRCh37
NC_000011.8:g.86341147_86341149del NCBI36
NG_011752.1:g.7934_7936del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.298_300del (FZD4) MANE Select ENSP00000434034.1:p.Ser100del
ENST00000531380.1:c.298_300del (FZD4) ENSP00000434034.1:p.Ser100del
ENST00000532234.5:c.*1450_*1452del (PRSS23) ENSP00000436676.1:n.*1450_*1452del
ENST00000533902.2:c.*1172_*1174del (PRSS23) ENSP00000437268.1:n.*1172_*1174del
NM_012193.3:c.298_300del (FZD4) NP_036325.2:p.Ser100del
NR_120591.1:n.2122_2124del (PRSS23)
NR_120592.1:n.1871_1873del (PRSS23)
NR_120591.2:n.1820_1822del (PRSS23)
NR_120592.2:n.1569_1571del (PRSS23)
NM_012193.4:c.298_300del (FZD4) MANE Select NP_036325.2:p.Ser100del
NR_120591.3:n.1820_1822del (PRSS23)