Canonical Allele Identifier: CA382011159

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951294C>A , CM000673.2:g.86951294C>A GRCh38
NC_000011.9:g.86662336C>A , CM000673.1:g.86662336C>A GRCh37
NC_000011.8:g.86339984C>A NCBI36
NG_011752.1:g.9098G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1462G>T (FZD4) MANE Select ENSP00000434034.1:p.Gly488Cys
ENST00000528769.5:n.351C>A (PRSS23)
ENST00000531380.1:c.1462G>T (FZD4) ENSP00000434034.1:p.Gly488Cys
ENST00000531521.1:n.465C>A (PRSS23)
ENST00000532234.5:c.*287C>A (PRSS23) ENSP00000436676.1:n.*287C>A
ENST00000533902.2:c.*9C>A (PRSS23) ENSP00000437268.1:n.*9C>A
NM_012193.3:c.1462G>T (FZD4) NP_036325.2:p.Gly488Cys
NR_120591.1:n.959C>A (PRSS23)
NR_120592.1:n.708C>A (PRSS23)
NR_120591.2:n.657C>A (PRSS23)
NR_120592.2:n.406C>A (PRSS23)
NM_012193.4:c.1462G>T (FZD4) MANE Select NP_036325.2:p.Gly488Cys
NR_120591.3:n.657C>A (PRSS23)