Canonical Allele Identifier: CA681337946

Linked Data

dbSNP Id: rs1344605261

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950749_86950758dup , CM000673.2:g.86950749_86950758dup GRCh38
NC_000011.9:g.86661791_86661800dup , CM000673.1:g.86661791_86661800dup GRCh37
NC_000011.8:g.86339439_86339448dup NCBI36
NG_011752.1:g.9635_9644dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*385_*394dup (FZD4) MANE Select ENSP00000434034.1:n.*385_*394dup
ENST00000528769.5:n.272+250_272+259dup (PRSS23)
ENST00000531380.1:c.*385_*394dup (FZD4) ENSP00000434034.1:n.*385_*394dup
ENST00000531521.1:n.386+250_386+259dup (PRSS23)
ENST00000532234.5:c.*208+250_*208+259dup (PRSS23) ENSP00000436676.1:n.*208+250_*208+259dup
ENST00000533902.2:c.207-467_207-458dup (PRSS23) ENSP00000437268.1:n.207-467_207-458dup
NM_012193.3:c.*385_*394dup (FZD4) NP_036325.2:n.*385_*394dup
NR_120591.1:n.880+250_880+259dup (PRSS23)
NR_120592.1:n.630-467_630-458dup (PRSS23)
NR_120591.2:n.578+250_578+259dup (PRSS23)
NR_120592.2:n.328-467_328-458dup (PRSS23)
NM_012193.4:c.*385_*394dup (FZD4) MANE Select NP_036325.2:n.*385_*394dup
NR_120591.3:n.578+250_578+259dup (PRSS23)