Canonical Allele Identifier: CA382017542

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86952466A>T , CM000673.2:g.86952466A>T GRCh38
NC_000011.9:g.86663508A>T , CM000673.1:g.86663508A>T GRCh37
NC_000011.8:g.86341156A>T NCBI36
NG_011752.1:g.7926T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.290T>A (FZD4) MANE Select ENSP00000434034.1:p.Phe97Tyr
ENST00000531380.1:c.290T>A (FZD4) ENSP00000434034.1:p.Phe97Tyr
ENST00000532234.5:c.*1459A>T (PRSS23) ENSP00000436676.1:n.*1459A>T
ENST00000533902.2:c.*1181A>T (PRSS23) ENSP00000437268.1:n.*1181A>T
NM_012193.3:c.290T>A (FZD4) NP_036325.2:p.Phe97Tyr
NR_120591.1:n.2131A>T (PRSS23)
NR_120592.1:n.1880A>T (PRSS23)
NR_120591.2:n.1829A>T (PRSS23)
NR_120592.2:n.1578A>T (PRSS23)
NM_012193.4:c.290T>A (FZD4) MANE Select NP_036325.2:p.Phe97Tyr
NR_120591.3:n.1829A>T (PRSS23)