Canonical Allele Identifier: CA382011693

Linked Data

dbSNP Id: rs1173578739

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951425T>A , CM000673.2:g.86951425T>A GRCh38
NC_000011.9:g.86662467T>A , CM000673.1:g.86662467T>A GRCh37
NC_000011.8:g.86340115T>A NCBI36
NG_011752.1:g.8967A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1331A>T (FZD4) MANE Select ENSP00000434034.1:p.Tyr444Phe
ENST00000531380.1:c.1331A>T (FZD4) ENSP00000434034.1:p.Tyr444Phe
ENST00000531521.1:n.596T>A (PRSS23)
ENST00000532234.5:c.*418T>A (PRSS23) ENSP00000436676.1:n.*418T>A
ENST00000533902.2:c.*140T>A (PRSS23) ENSP00000437268.1:n.*140T>A
NM_012193.3:c.1331A>T (FZD4) NP_036325.2:p.Tyr444Phe
NR_120591.1:n.1090T>A (PRSS23)
NR_120592.1:n.839T>A (PRSS23)
NR_120591.2:n.788T>A (PRSS23)
NR_120592.2:n.537T>A (PRSS23)
NM_012193.4:c.1331A>T (FZD4) MANE Select NP_036325.2:p.Tyr444Phe
NR_120591.3:n.788T>A (PRSS23)