Canonical Allele Identifier: CA382016155

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952284A>G , CM000673.2:g.86952284A>G GRCh38
NC_000011.9:g.86663326A>G , CM000673.1:g.86663326A>G GRCh37
NC_000011.8:g.86340974A>G NCBI36
NG_011752.1:g.8108T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.472T>C (FZD4) MANE Select ENSP00000434034.1:p.Cys158Arg
ENST00000531380.1:c.472T>C (FZD4) ENSP00000434034.1:p.Cys158Arg
ENST00000532234.5:c.*1277A>G (PRSS23) ENSP00000436676.1:n.*1277A>G
ENST00000533902.2:c.*999A>G (PRSS23) ENSP00000437268.1:n.*999A>G
NM_012193.3:c.472T>C (FZD4) NP_036325.2:p.Cys158Arg
NR_120591.1:n.1949A>G (PRSS23)
NR_120592.1:n.1698A>G (PRSS23)
NR_120591.2:n.1647A>G (PRSS23)
NR_120592.2:n.1396A>G (PRSS23)
NM_012193.4:c.472T>C (FZD4) MANE Select NP_036325.2:p.Cys158Arg
NR_120591.3:n.1647A>G (PRSS23)