Canonical Allele Identifier: CA1988804010

Linked Data

dbSNP Id: rs1949256662

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86947854_86947871del , CM000673.2:g.86947854_86947871del GRCh38
NC_000011.9:g.86658896_86658913del , CM000673.1:g.86658896_86658913del GRCh37
NC_000011.8:g.86336544_86336561del NCBI36
NG_011752.1:g.12525_12542del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*3275_*3292del (FZD4) MANE Select ENSP00000434034.1:n.*3275_*3292del
ENST00000528769.5:n.129-2502_129-2485del (PRSS23)
ENST00000531380.1:c.*3275_*3292del (FZD4) ENSP00000434034.1:n.*3275_*3292del
ENST00000531521.1:n.243-2502_243-2485del (PRSS23)
ENST00000532234.5:c.*65-2502_*65-2485del (PRSS23) ENSP00000436676.1:n.*65-2502_*65-2485del
ENST00000533902.2:c.207-3362_207-3345del (PRSS23) ENSP00000437268.1:n.207-3362_207-3345del
NM_012193.3:c.*3275_*3292del (FZD4) NP_036325.2:n.*3275_*3292del
NR_120591.1:n.737-2502_737-2485del (PRSS23)
NR_120592.1:n.630-3362_630-3345del (PRSS23)
NR_120591.2:n.435-2502_435-2485del (PRSS23)
NR_120592.2:n.328-3362_328-3345del (PRSS23)
NM_012193.4:c.*3275_*3292del (FZD4) MANE Select NP_036325.2:n.*3275_*3292del
NR_120591.3:n.435-2502_435-2485del (PRSS23)