Canonical Allele Identifier: CA2615455489

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952054_86952073del , CM000673.2:g.86952054_86952073del GRCh38
NC_000011.9:g.86663096_86663115del , CM000673.1:g.86663096_86663115del GRCh37
NC_000011.8:g.86340744_86340763del NCBI36
NG_011752.1:g.8323_8342del

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.687_706del (FZD4) MANE Select ENSP00000434034.1:p.Cys230HisfsTer11
ENST00000531380.1:c.687_706del (FZD4) ENSP00000434034.1:p.Cys230HisfsTer11
ENST00000532234.5:c.*1047_*1066del (PRSS23) ENSP00000436676.1:n.*1047_*1066del
ENST00000533902.2:c.*769_*788del (PRSS23) ENSP00000437268.1:n.*769_*788del
NM_012193.3:c.687_706del (FZD4) NP_036325.2:p.Cys230HisfsTer11
NR_120591.1:n.1719_1738del (PRSS23)
NR_120592.1:n.1468_1487del (PRSS23)
NR_120591.2:n.1417_1436del (PRSS23)
NR_120592.2:n.1166_1185del (PRSS23)
NM_012193.4:c.687_706del (FZD4) MANE Select NP_036325.2:p.Cys230HisfsTer11
NR_120591.3:n.1417_1436del (PRSS23)