Canonical Allele Identifier: CA382011098

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86951275C>T , CM000673.2:g.86951275C>T GRCh38
NC_000011.9:g.86662317C>T , CM000673.1:g.86662317C>T GRCh37
NC_000011.8:g.86339965C>T NCBI36
NG_011752.1:g.9117G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000531380.2:c.1481G>A (FZD4) MANE Select ENSP00000434034.1:p.Trp494Ter
ENST00000528769.5:n.332C>T (PRSS23)
ENST00000531380.1:c.1481G>A (FZD4) ENSP00000434034.1:p.Trp494Ter
ENST00000531521.1:n.446C>T (PRSS23)
ENST00000532234.5:c.*268C>T (PRSS23) ENSP00000436676.1:n.*268C>T
ENST00000533902.2:c.266C>T (PRSS23) ENSP00000437268.1:p.Pro89Leu
NM_012193.3:c.1481G>A (FZD4) NP_036325.2:p.Trp494Ter
NR_120591.1:n.940C>T (PRSS23)
NR_120592.1:n.689C>T (PRSS23)
NR_120591.2:n.638C>T (PRSS23)
NR_120592.2:n.387C>T (PRSS23)
NM_012193.4:c.1481G>A (FZD4) MANE Select NP_036325.2:p.Trp494Ter
NR_120591.3:n.638C>T (PRSS23)