Canonical Allele Identifier: CA382016623

Linked Data

dbSNP Id: rs1317445197

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952339C>T , CM000673.2:g.86952339C>T GRCh38
NC_000011.9:g.86663381C>T , CM000673.1:g.86663381C>T GRCh37
NC_000011.8:g.86341029C>T NCBI36
NG_011752.1:g.8053G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.417G>A (FZD4) MANE Select ENSP00000434034.1:p.Trp139Ter
ENST00000531380.1:c.417G>A (FZD4) ENSP00000434034.1:p.Trp139Ter
ENST00000532234.5:c.*1332C>T (PRSS23) ENSP00000436676.1:n.*1332C>T
ENST00000533902.2:c.*1054C>T (PRSS23) ENSP00000437268.1:n.*1054C>T
NM_012193.3:c.417G>A (FZD4) NP_036325.2:p.Trp139Ter
NR_120591.1:n.2004C>T (PRSS23)
NR_120592.1:n.1753C>T (PRSS23)
NR_120591.2:n.1702C>T (PRSS23)
NR_120592.2:n.1451C>T (PRSS23)
NM_012193.4:c.417G>A (FZD4) MANE Select NP_036325.2:p.Trp139Ter
NR_120591.3:n.1702C>T (PRSS23)