Canonical Allele Identifier: CA1988807114

Linked Data

dbSNP Id: rs1949284136

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950839G>A , CM000673.2:g.86950839G>A GRCh38
NC_000011.9:g.86661881G>A , CM000673.1:g.86661881G>A GRCh37
NC_000011.8:g.86339529G>A NCBI36
NG_011752.1:g.9553C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*303C>T (FZD4) MANE Select ENSP00000434034.1:n.*303C>T
ENST00000528769.5:n.272+340G>A (PRSS23)
ENST00000531380.1:c.*303C>T (FZD4) ENSP00000434034.1:n.*303C>T
ENST00000531521.1:n.386+340G>A (PRSS23)
ENST00000532234.5:c.*208+340G>A (PRSS23) ENSP00000436676.1:n.*208+340G>A
ENST00000533902.2:c.207-377G>A (PRSS23) ENSP00000437268.1:n.207-377G>A
NM_012193.3:c.*303C>T (FZD4) NP_036325.2:n.*303C>T
NR_120591.1:n.880+340G>A (PRSS23)
NR_120592.1:n.630-377G>A (PRSS23)
NR_120591.2:n.578+340G>A (PRSS23)
NR_120592.2:n.328-377G>A (PRSS23)
NM_012193.4:c.*303C>T (FZD4) MANE Select NP_036325.2:n.*303C>T
NR_120591.3:n.578+340G>A (PRSS23)