Canonical Allele Identifier: CA382016692

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952347A>G , CM000673.2:g.86952347A>G GRCh38
NC_000011.9:g.86663389A>G , CM000673.1:g.86663389A>G GRCh37
NC_000011.8:g.86341037A>G NCBI36
NG_011752.1:g.8045T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.409T>C (FZD4) MANE Select ENSP00000434034.1:p.Phe137Leu
ENST00000531380.1:c.409T>C (FZD4) ENSP00000434034.1:p.Phe137Leu
ENST00000532234.5:c.*1340A>G (PRSS23) ENSP00000436676.1:n.*1340A>G
ENST00000533902.2:c.*1062A>G (PRSS23) ENSP00000437268.1:n.*1062A>G
NM_012193.3:c.409T>C (FZD4) NP_036325.2:p.Phe137Leu
NR_120591.1:n.2012A>G (PRSS23)
NR_120592.1:n.1761A>G (PRSS23)
NR_120591.2:n.1710A>G (PRSS23)
NR_120592.2:n.1459A>G (PRSS23)
NM_012193.4:c.409T>C (FZD4) MANE Select NP_036325.2:p.Phe137Leu
NR_120591.3:n.1710A>G (PRSS23)