Canonical Allele Identifier: CA382016077

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952275C>T , CM000673.2:g.86952275C>T GRCh38
NC_000011.9:g.86663317C>T , CM000673.1:g.86663317C>T GRCh37
NC_000011.8:g.86340965C>T NCBI36
NG_011752.1:g.8117G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.481G>A (FZD4) MANE Select ENSP00000434034.1:p.Gly161Arg
ENST00000531380.1:c.481G>A (FZD4) ENSP00000434034.1:p.Gly161Arg
ENST00000532234.5:c.*1268C>T (PRSS23) ENSP00000436676.1:n.*1268C>T
ENST00000533902.2:c.*990C>T (PRSS23) ENSP00000437268.1:n.*990C>T
NM_012193.3:c.481G>A (FZD4) NP_036325.2:p.Gly161Arg
NR_120591.1:n.1940C>T (PRSS23)
NR_120592.1:n.1689C>T (PRSS23)
NR_120591.2:n.1638C>T (PRSS23)
NR_120592.2:n.1387C>T (PRSS23)
NM_012193.4:c.481G>A (FZD4) MANE Select NP_036325.2:p.Gly161Arg
NR_120591.3:n.1638C>T (PRSS23)