Canonical Allele Identifier: CA382011452

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951375T>A , CM000673.2:g.86951375T>A GRCh38
NC_000011.9:g.86662417T>A , CM000673.1:g.86662417T>A GRCh37
NC_000011.8:g.86340065T>A NCBI36
NG_011752.1:g.9017A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1381A>T (FZD4) MANE Select ENSP00000434034.1:p.Asn461Tyr
ENST00000528769.5:n.432T>A (PRSS23)
ENST00000531380.1:c.1381A>T (FZD4) ENSP00000434034.1:p.Asn461Tyr
ENST00000531521.1:n.546T>A (PRSS23)
ENST00000532234.5:c.*368T>A (PRSS23) ENSP00000436676.1:n.*368T>A
ENST00000533902.2:c.*90T>A (PRSS23) ENSP00000437268.1:n.*90T>A
NM_012193.3:c.1381A>T (FZD4) NP_036325.2:p.Asn461Tyr
NR_120591.1:n.1040T>A (PRSS23)
NR_120592.1:n.789T>A (PRSS23)
NR_120591.2:n.738T>A (PRSS23)
NR_120592.2:n.487T>A (PRSS23)
NM_012193.4:c.1381A>T (FZD4) MANE Select NP_036325.2:p.Asn461Tyr
NR_120591.3:n.738T>A (PRSS23)