Canonical Allele Identifier: CA476144849

Linked Data

dbSNP Id: rs1189131795

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952459A>G , CM000673.2:g.86952459A>G GRCh38
NC_000011.9:g.86663501A>G , CM000673.1:g.86663501A>G GRCh37
NC_000011.8:g.86341149A>G NCBI36
NG_011752.1:g.7933T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.297T>C (FZD4) MANE Select ENSP00000434034.1:p.Cys99=
ENST00000531380.1:c.297T>C (FZD4) ENSP00000434034.1:p.Cys99=
ENST00000532234.5:c.*1452A>G (PRSS23) ENSP00000436676.1:n.*1452A>G
ENST00000533902.2:c.*1174A>G (PRSS23) ENSP00000437268.1:n.*1174A>G
NM_012193.3:c.297T>C (FZD4) NP_036325.2:p.Cys99=
NR_120591.1:n.2124A>G (PRSS23)
NR_120592.1:n.1873A>G (PRSS23)
NR_120591.2:n.1822A>G (PRSS23)
NR_120592.2:n.1571A>G (PRSS23)
NM_012193.4:c.297T>C (FZD4) MANE Select NP_036325.2:p.Cys99=
NR_120591.3:n.1822A>G (PRSS23)