Canonical Allele Identifier: CA382010991

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951235A>C , CM000673.2:g.86951235A>C GRCh38
NC_000011.9:g.86662277A>C , CM000673.1:g.86662277A>C GRCh37
NC_000011.8:g.86339925A>C NCBI36
NG_011752.1:g.9157T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1521T>G (FZD4) MANE Select ENSP00000434034.1:p.Cys507Trp
ENST00000528769.5:n.292A>C (PRSS23)
ENST00000531380.1:c.1521T>G (FZD4) ENSP00000434034.1:p.Cys507Trp
ENST00000531521.1:n.406A>C (PRSS23)
ENST00000532234.5:c.*228A>C (PRSS23) ENSP00000436676.1:n.*228A>C
ENST00000533902.2:c.226A>C (PRSS23) ENSP00000437268.1:p.Thr76Pro
NM_012193.3:c.1521T>G (FZD4) NP_036325.2:p.Cys507Trp
NR_120591.1:n.900A>C (PRSS23)
NR_120592.1:n.649A>C (PRSS23)
NR_120591.2:n.598A>C (PRSS23)
NR_120592.2:n.347A>C (PRSS23)
NM_012193.4:c.1521T>G (FZD4) MANE Select NP_036325.2:p.Cys507Trp
NR_120591.3:n.598A>C (PRSS23)