Canonical Allele Identifier: CA2615460865

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86950803C>T , CM000673.2:g.86950803C>T GRCh38
NC_000011.9:g.86661845C>T , CM000673.1:g.86661845C>T GRCh37
NC_000011.8:g.86339493C>T NCBI36
NG_011752.1:g.9589G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.*339G>A (FZD4) MANE Select ENSP00000434034.1:n.*339G>A
ENST00000528769.5:n.272+304C>T (PRSS23)
ENST00000531380.1:c.*339G>A (FZD4) ENSP00000434034.1:n.*339G>A
ENST00000531521.1:n.386+304C>T (PRSS23)
ENST00000532234.5:c.*208+304C>T (PRSS23) ENSP00000436676.1:n.*208+304C>T
ENST00000533902.2:c.207-413C>T (PRSS23) ENSP00000437268.1:n.207-413C>T
NM_012193.3:c.*339G>A (FZD4) NP_036325.2:n.*339G>A
NR_120591.1:n.880+304C>T (PRSS23)
NR_120592.1:n.630-413C>T (PRSS23)
NR_120591.2:n.578+304C>T (PRSS23)
NR_120592.2:n.328-413C>T (PRSS23)
NM_012193.4:c.*339G>A (FZD4) MANE Select NP_036325.2:n.*339G>A
NR_120591.3:n.578+304C>T (PRSS23)