Canonical Allele Identifier: CA382016729

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952353A>C , CM000673.2:g.86952353A>C GRCh38
NC_000011.9:g.86663395A>C , CM000673.1:g.86663395A>C GRCh37
NC_000011.8:g.86341043A>C NCBI36
NG_011752.1:g.8039T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.403T>G (FZD4) MANE Select ENSP00000434034.1:p.Phe135Val
ENST00000531380.1:c.403T>G (FZD4) ENSP00000434034.1:p.Phe135Val
ENST00000532234.5:c.*1346A>C (PRSS23) ENSP00000436676.1:n.*1346A>C
ENST00000533902.2:c.*1068A>C (PRSS23) ENSP00000437268.1:n.*1068A>C
NM_012193.3:c.403T>G (FZD4) NP_036325.2:p.Phe135Val
NR_120591.1:n.2018A>C (PRSS23)
NR_120592.1:n.1767A>C (PRSS23)
NR_120591.2:n.1716A>C (PRSS23)
NR_120592.2:n.1465A>C (PRSS23)
NM_012193.4:c.403T>G (FZD4) MANE Select NP_036325.2:p.Phe135Val
NR_120591.3:n.1716A>C (PRSS23)