Canonical Allele Identifier: CA681336433

Linked Data

dbSNP Id: rs1233994784

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86948062_86948071del , CM000673.2:g.86948062_86948071del GRCh38
NC_000011.9:g.86659104_86659113del , CM000673.1:g.86659104_86659113del GRCh37
NC_000011.8:g.86336752_86336761del NCBI36
NG_011752.1:g.12322_12331del

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*3072_*3081del (FZD4) MANE Select ENSP00000434034.1:n.*3072_*3081del
ENST00000528769.5:n.129-2294_129-2285del (PRSS23)
ENST00000531380.1:c.*3072_*3081del (FZD4) ENSP00000434034.1:n.*3072_*3081del
ENST00000531521.1:n.243-2294_243-2285del (PRSS23)
ENST00000532234.5:c.*65-2294_*65-2285del (PRSS23) ENSP00000436676.1:n.*65-2294_*65-2285del
ENST00000533902.2:c.207-3154_207-3145del (PRSS23) ENSP00000437268.1:n.207-3154_207-3145del
NM_012193.3:c.*3072_*3081del (FZD4) NP_036325.2:n.*3072_*3081del
NR_120591.1:n.737-2294_737-2285del (PRSS23)
NR_120592.1:n.630-3154_630-3145del (PRSS23)
NR_120591.2:n.435-2294_435-2285del (PRSS23)
NR_120592.2:n.328-3154_328-3145del (PRSS23)
NM_012193.4:c.*3072_*3081del (FZD4) MANE Select NP_036325.2:n.*3072_*3081del
NR_120591.3:n.435-2294_435-2285del (PRSS23)