Canonical Allele Identifier: CA382010981

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951232G>A , CM000673.2:g.86951232G>A GRCh38
NC_000011.9:g.86662274G>A , CM000673.1:g.86662274G>A GRCh37
NC_000011.8:g.86339922G>A NCBI36
NG_011752.1:g.9160C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000531380.2:c.1524C>T (FZD4) MANE Select ENSP00000434034.1:p.Ser508=
ENST00000528769.5:n.289G>A (PRSS23)
ENST00000531380.1:c.1524C>T (FZD4) ENSP00000434034.1:p.Ser508=
ENST00000531521.1:n.403G>A (PRSS23)
ENST00000532234.5:c.*225G>A (PRSS23) ENSP00000436676.1:n.*225G>A
ENST00000533902.2:c.223G>A (PRSS23) ENSP00000437268.1:p.Gly75Arg
NM_012193.3:c.1524C>T (FZD4) NP_036325.2:p.Ser508=
NR_120591.1:n.897G>A (PRSS23)
NR_120592.1:n.646G>A (PRSS23)
NR_120591.2:n.595G>A (PRSS23)
NR_120592.2:n.344G>A (PRSS23)
NM_012193.4:c.1524C>T (FZD4) MANE Select NP_036325.2:p.Ser508=
NR_120591.3:n.595G>A (PRSS23)