Canonical Allele Identifier: CA2600523646

Linked Data

dbSNP Id: rs2135034575

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86947874del , CM000673.2:g.86947874del GRCh38
NC_000011.9:g.86658916del , CM000673.1:g.86658916del GRCh37
NC_000011.8:g.86336564del NCBI36
NG_011752.1:g.12519del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*3269del (FZD4) MANE Select ENSP00000434034.1:n.*3269del
ENST00000528769.5:n.129-2482del (PRSS23)
ENST00000531380.1:c.*3269del (FZD4) ENSP00000434034.1:n.*3269del
ENST00000531521.1:n.243-2482del (PRSS23)
ENST00000532234.5:c.*65-2482del (PRSS23) ENSP00000436676.1:n.*65-2482del
ENST00000533902.2:c.207-3342del (PRSS23) ENSP00000437268.1:n.207-3342del
NM_012193.3:c.*3269del (FZD4) NP_036325.2:n.*3269del
NR_120591.1:n.737-2482del (PRSS23)
NR_120592.1:n.630-3342del (PRSS23)
NR_120591.2:n.435-2482del (PRSS23)
NR_120592.2:n.328-3342del (PRSS23)
NM_012193.4:c.*3269del (FZD4) MANE Select NP_036325.2:n.*3269del
NR_120591.3:n.435-2482del (PRSS23)